Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35
Zinc Oxide
Offspring Beauty Co.
Human Otc Drug
NDC 73690-027Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35 also known as Zinc Oxide is a human otc drug labeled by 'Offspring Beauty Co.'. National Drug Code (NDC) number for Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35 is 73690-027. This drug is available in dosage form of Lotion. The names of the active, medicinal ingredients in Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35 drug includes Zinc Oxide - 15.2 g/100mL . The currest status of Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35 drug is Active.
Drug Information:
| Drug NDC: | 73690-027 |
| 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: | Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35 |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| 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: | Zinc Oxide |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Offspring Beauty Co. |
| 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: | ZINC OXIDE - 15.2 g/100mL
|
| 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 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 Oct, 2021 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 22 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: | M020 |
| 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, 2023 |
| 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: | Offspring Beauty Co.
|
| 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: | 0810002111372
|
| UPC stands for Universal Product Code. |
| UNII: | SOI2LOH54Z
|
| 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 NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 73690-027-01 | 50 mL in 1 TUBE (73690-027-01) | 01 Oct, 2021 | N/A | No |
| 73690-027-02 | 75 mL in 1 TUBE (73690-027-02) | 01 Apr, 2022 | N/A | No |
| 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. |
Purpose:
Purpose sunscreen
Sunscreen
Product Elements:
Versed guards up daily mineral sunscreen broad spectrum spf 35 zinc oxide c18-c21 alkane erythritol cetostearyl alcohol sodium stearoyl glutamate citric acid monohydrate coco glucoside caprylhydroxamic acid hyaluronate sodium docosanol polyhydroxystearic acid (2300 mw) cetyl alcohol propanediol glycerin apple xanthan gum crithmum maritimum whole maltodextrin isodecyl neopentanoate diheptyl succinate capryloyl glycerin/sebacic acid copolymer (2000 mpa.s) ferric oxide red medium-chain triglycerides caprylyl glycol levomenol hydrolyzed jojoba esters (acid form) sodium gluconate octyldodecyl oleate water arachidyl alcohol tocopherol ethyl ferulate aloe vera leaf butyloctyl salicylate zinc oxide zinc oxide ferric oxide yellow
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. keep out of reach of children. if swallowed, get medical help or contact a poison control center right away.
Dosage and Administration:
Directions apply liberally and evenly 15 minutes before sun exposure reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating, immediately after toweling drying, and at least every 2 hours children under 6 months of age: ask a doctor 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 othe sun protection measures including: limit time in sun, especially from 10 a.m. to 2 p.m. and wear long-sleeved shirts, pants, hats, and sunglasses
Package Label Principal Display Panel:
75 ml tube & carton 1 2
50 ml tube & carton 6 7