Pca Skin Body Hydrator Spf30
Zinc Oxide And Octinoxate
Cp Skin Health Group, Inc
Human Otc Drug
NDC 68726-167Pca Skin Body Hydrator Spf30 also known as Zinc Oxide And Octinoxate is a human otc drug labeled by 'Cp Skin Health Group, Inc'. National Drug Code (NDC) number for Pca Skin Body Hydrator Spf30 is 68726-167. This drug is available in dosage form of Lotion. The names of the active, medicinal ingredients in Pca Skin Body Hydrator Spf30 drug includes Octinoxate - 7.5 g/100g Zinc Oxide - 9.8 g/100g . The currest status of Pca Skin Body Hydrator Spf30 drug is Active.
Drug Information:
| Drug NDC: | 68726-167 |
| 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: | Pca Skin Body Hydrator Spf30 |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Proprietary Name Base: | Pca Skin Body Hydrator |
| The base of the Brand/Proprietary name excluding its suffix. |
| Proprietary Name Suffix: | SPF30 |
| 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: | Zinc Oxide And Octinoxate |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Cp Skin Health Group, 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 - 7.5 g/100g
ZINC OXIDE - 9.8 g/100g
|
| 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 Oct, 2010 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 10 May, 2026 |
| 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, 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: | CP SKIN Health Group, 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. |
| UNII: | 4Y5P7MUD51
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 |
|---|
| 68726-167-02 | 48 g in 1 BOTTLE (68726-167-02) | 01 Oct, 2010 | N/A | No |
| 68726-167-04 | 1 TUBE in 1 CARTON (68726-167-04) / 9 g in 1 TUBE (68726-167-03) | 01 Oct, 2010 | N/A | No |
| 68726-167-05 | 1 BOTTLE in 1 CARTON (68726-167-05) / 198.4 g in 1 BOTTLE (68726-167-01) | 01 Oct, 2010 | 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. |
Product Elements:
Pca skin body hydrator spf30 zinc oxide and octinoxate water glycerin cyclomethicone 5 butylene glycol cetostearyl alcohol caffeine polysorbate 20 cellulose, microcrystalline carboxymethylcellulose sodium aloe vera leaf dimethicone .alpha.-tocopherol acetate, d- vitamin a palmitate glycyrrhiza glabra morus alba root bark lactic acid arginine phenoxyethanol caprylyl glycol ethylhexylglycerin hexylene glycol citrus paradisi seed alcohol milk thistle kojic acid sodium hydroxide zinc oxide zinc oxide octinoxate octinoxate
Indications and Usage:
Uses: provides high protection against sunburn.
Warnings:
Warnings: for external use only. keep out of eyes. rinse with water to remove. stop use and consult a physician if skin rash and irritation develops and lasts.
Dosage and Administration:
Directions: for use by adults and children six months and older. apply liberally to exposed areas at least 30 minutes prior to sun exposure. reapply every two hours or as needed after swimming or perspiring. consult a physician prior to use on children under six months of age. other information: sun alert. limiting sun exposure, wearing protecting clothing and using sunscreens may reduce the risks of skin aging, skin cancer and other harmful effects of the sun.
Package Label Principal Display Panel:
Perfectingspfuc