Neutrogena Healthy Skin Anti-aging Perfector Sunscreen Broad Spectrum Spf 20 Medium To Deep 60

Octinoxate And Octisalate


Johnson & Johnson Consumer Inc.
Human Otc Drug
NDC 69968-0081
Neutrogena Healthy Skin Anti-aging Perfector Sunscreen Broad Spectrum Spf 20 Medium To Deep 60 also known as Octinoxate And Octisalate is a human otc drug labeled by 'Johnson & Johnson Consumer Inc.'. National Drug Code (NDC) number for Neutrogena Healthy Skin Anti-aging Perfector Sunscreen Broad Spectrum Spf 20 Medium To Deep 60 is 69968-0081. This drug is available in dosage form of Lotion. The names of the active, medicinal ingredients in Neutrogena Healthy Skin Anti-aging Perfector Sunscreen Broad Spectrum Spf 20 Medium To Deep 60 drug includes Octinoxate - 70 mg/mL Octisalate - 30 mg/mL . The currest status of Neutrogena Healthy Skin Anti-aging Perfector Sunscreen Broad Spectrum Spf 20 Medium To Deep 60 drug is Active.

Drug Information:

Drug NDC: 69968-0081
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Neutrogena Healthy Skin Anti-aging Perfector Sunscreen Broad Spectrum Spf 20 Medium To Deep 60
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base: Neutrogena Healthy Skin Anti-aging Perfector Sunscreen Broad Spectrum Spf 20
The base of the Brand/Proprietary name excluding its suffix.
Proprietary Name Suffix: Medium to Deep 60
A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
Product Type: Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Octinoxate And Octisalate
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Johnson & Johnson Consumer Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Lotion
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:OCTINOXATE - 70 mg/mL
OCTISALATE - 30 mg/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:TOPICAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: OTC MONOGRAPH NOT FINAL
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date: 01 Nov, 2015
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 21 Dec, 2025
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number: part352
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Listing Expiration Date: 31 Dec, 2024
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Johnson & Johnson Consumer Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UPC:0086800437963
0086800437932
0086800437949
0086800437970
0086800437987
0086800437956
UPC stands for Universal Product Code.
UNII:4Y5P7MUD51
4X49Y0596W
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
69968-0081-130 mL in 1 BOTTLE (69968-0081-1)01 Nov, 2015N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.
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Purpose:

Purpose sunscreen

Product Elements:

Neutrogena healthy skin anti-aging perfector sunscreen broad spectrum spf 20 ivory to fair 10 octinoxate and octisalate water titanium dioxide isopropyl isostearate cyclomethicone 5 dimethicone butylene glycol glyceryl monostearate cetyl alcohol cetostearyl alcohol peg-75 stearate lauroyl lysine .alpha.-tocopherol acetate black olive butylated hydroxytoluene erythorbic acid levomenol vitamin a palmitate retinol arginine silicon dioxide polysorbate 20 peg-100 stearate isostearyl palmitate betasizofiran dimethicone/vinyl dimethicone crosspolymer (soft particle) ceteth-20 steareth-20 edetate sodium ferric oxide red methylparaben propylparaben ethylparaben phenoxyethanol octinoxate octinoxate octisalate octisalate neutrogena healthy skin anti-aging perfector sunscreen broad spectrum spf 20 fair to light 20 octinoxate and octisalate peg-100 stearate isostearyl palmitate betasizofiran dimethicone/vinyl dimethicone crosspolymer (soft particle) ceteth-20 steareth-20 edetate sodium ferric oxide red methylparaben propylparaben ethylparaben phenoxyethanol octinoxate octinoxate octisalate octisalate water titanium dioxide isopropyl isostearate cyclomethicone 5 dimethicone butylene glycol glyceryl monostearate cetyl alcohol cetostearyl alcohol peg-75 stearate lauroyl lysine .alpha.-tocopherol acetate black olive butylated hydroxytoluene erythorbic acid levomenol vitamin a palmitate retinol arginine silicon dioxide polysorbate 20 neutrogena healthy skin anti-aging perfector sunscreen broad spectrum spf 20 light to neutral 30 octinoxate and octisalate water titanium dioxide isopropyl isostearate cyclomethicone 5 dimethicone butylene glycol glyceryl monostearate cetyl alcohol cetostearyl alcohol peg-75 stearate lauroyl lysine .alpha.-tocopherol acetate black olive butylated hydroxytoluene erythorbic acid levomenol vitamin a palmitate retinol arginine silicon dioxide polysorbate 20 peg-100 stearate isostearyl palmitate betasizofiran dimethicone/vinyl dimethicone crosspolymer (soft particle) ceteth-20 steareth-20 edetate sodium ferric oxide red methylparaben propylparaben ethylparaben phenoxyethanol octinoxate octinoxate octisalate octisalate neutrogena healthy skin anti-aging perfector sunscreen broad spectrum spf 20 neutral to tan 40 octinoxate and octisalate water titanium dioxide isopropyl isostearate cyclomethicone 5 dimethicone butylene glycol glyceryl monostearate cetyl alcohol cetostearyl alcohol peg-75 stearate lauroyl lysine .alpha.-tocopherol acetate black olive butylated hydroxytoluene erythorbic acid levomenol vitamin a palmitate retinol arginine silicon dioxide polysorbate 20 peg-100 stearate isostearyl palmitate betasizofiran dimethicone/vinyl dimethicone crosspolymer (soft particle) ceteth-20 steareth-20 edetate sodium ferric oxide red methylparaben propylparaben ethylparaben phenoxyethanol octinoxate octinoxate octisalate octisalate neutrogena healthy skin anti-aging perfector sunscreen broad spectrum spf 20 tan to medium 50 octinoxate and octisalate isopropyl isostearate cyclomethicone 5 dimethicone butylene glycol glyceryl monostearate cetyl alcohol cetostearyl alcohol peg-75 stearate lauroyl lysine .alpha.-tocopherol acetate black olive butylated hydroxytoluene erythorbic acid levomenol vitamin a palmitate retinol arginine silicon dioxide polysorbate 20 peg-100 stearate isostearyl palmitate betasizofiran dimethicone/vinyl dimethicone crosspolymer (soft particle) ceteth-20 steareth-20 edetate sodium ferric oxide red methylparaben propylparaben ethylparaben phenoxyethanol octinoxate octinoxate octisalate octisalate water titanium dioxide neutrogena healthy skin anti-aging perfector sunscreen broad spectrum spf 20 medium to deep 60 octinoxate and octisalate water titanium dioxide isopropyl isostearate cyclomethicone 5 dimethicone butylene glycol glyceryl monostearate cetyl alcohol cetostearyl alcohol peg-75 stearate lauroyl lysine .alpha.-tocopherol acetate black olive butylated hydroxytoluene erythorbic acid levomenol vitamin a palmitate retinol arginine silicon dioxide polysorbate 20 peg-100 stearate isostearyl palmitate betasizofiran dimethicone/vinyl dimethicone crosspolymer (soft particle) ceteth-20 steareth-20 edetate sodium ferric oxide red methylparaben propylparaben ethylparaben phenoxyethanol octinoxate octinoxate octisalate octisalate

Indications and Usage:

Uses helps prevent sunburn if used as directed with other sun protection measures (see directions ), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings:

Warnings for external use only do not use on damaged or broken skin when using this product keep out of eyes. rinse with water to remove. stop use and ask a doctor if rash occurs keep out of reach of children. if swallowed, get medical help or contact a poison control center right away

Do Not Use:

Warnings for external use only do not use on damaged or broken skin when using this product keep out of eyes. rinse with water to remove. stop use and ask a doctor if rash occurs keep out of reach of children. if swallowed, get medical help or contact a poison control center right away

When Using:

When using this product keep out of eyes. rinse with water to remove.

Dosage and Administration:

Directions apply liberally 15 minutes before sun exposure use a water resistant sunscreen if swimming or sweating reapply at least every 2 hours. sun protection measures. spending time in the sun increases your risk of skin cancer and early skin aging. to decrease this risk, regularly use a sunscreen with a broad spectrum spf value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m. – 2 p.m. wear long-sleeved shirts, pants, hats, and sunglasses children under 6 months of age: ask a doctor

Stop Use:

Stop use and ask a doctor if rash occurs

Package Label Principal Display Panel:

Principal display panel - 30 ml bottle label - ivory to fair 10 new neutrogena healthy skin ® anti-aging perfector ivory to fair 10 moisturizing retinol treatment with sunscreen broad spectrum spf 20 evens tone 1.0 fl oz (30 ml) principal display panel - 30 ml bottle label - ivory to fair 10

Principal display panel - 30 ml bottle label - fair to light 20 new neutrogena healthy skin ® anti-aging perfector fair to light 20 moisturizing retinol treatment with sunscreen broad spectrum spf 20 evens tone 1.0 fl oz (30 ml principal display panel - 30 ml bottle label - fair to light 20

Principal display panel - 30 ml bottle label - light to neutral 30 new neutrogena healthy skin ® anti-aging perfector light to neutral 30 moisturizing retinol treatment with sunscreen broad spectrum spf 20 evens tone 1.0 fl oz (30 ml) principal display panel - 30 ml bottle label - light to neutral 30

Principal display panel - 30 ml bottle label - neutral to tan 40 new neutrogena healthy skin ® anti-aging perfector neutral to tan 40 moisturizing retinol treatment with sunscreen broad spectrum spf 20 evens tone 1.0 fl oz (30 ml) principal display panel - 30 ml bottle label - neutral to tan 40

Principal display panel - 30 ml bottle label - tan to medium 50 new neutrogena healthy skin ® anti-aging perfector tan to medium 50 moisturizing retinol treatment with sunscreen broad spectrum spf 20 evens tone 1.0 fl oz (30 ml) principal display panel - 30 ml bottle label - tan to medium 50

Principal display panel - 30 ml bottle label - medium to deep 60 new neutrogena healthy skin ® anti-aging perfector medium to deep 60 moisturizing retinol treatment with sunscreen broad spectrum spf 20 evens tone 1.0 fl oz (30 ml) principal display panel - 30 ml bottle label - medium to deep 60

Further Questions:

Questions? call toll-free 800-480-4812 or 215-273-8755 ( collect). www.neutrogena.com


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.