NDC 79903-059 Spf Moisturizer

Spf Moisturizer

NDC Product Code 79903-059

NDC 79903-059-26

Package Description: 118 mL in 1 PACKAGE

NDC Product Information

Spf Moisturizer with NDC 79903-059 is a a human over the counter drug product labeled by Wal-mart Stores, Inc.. The generic name of Spf Moisturizer is spf moisturizer. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Wal-mart Stores, Inc.

Dosage Form: Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Spf Moisturizer Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • AVOBENZONE 3 mg/mL
  • OCTISALATE 5 mg/mL
  • OCTOCRYLENE 5 mg/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • SOYBEAN (UNII: L7HT8F1ZOD)
  • PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
  • ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
  • CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
  • CHLORPHENESIN (UNII: I670DAL4SZ)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • PANTHENOL (UNII: WV9CM0O67Z)
  • DOCOSANOL (UNII: 9G1OE216XY)
  • STEARETH-2 (UNII: V56DFE46J5)
  • STEARETH-21 (UNII: 53J3F32P58)
  • POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
  • POLYACRYLAMIDE (CROSSLINKED; 2 MOLE PERCENT BISACRYLAMIDE) (UNII: 9FPL31B58Q)
  • ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
  • EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
  • C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
  • LAURETH-7 (UNII: Z95S6G8201)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • MICA (UNII: V8A1AW0880)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Wal-mart Stores, Inc.
Labeler Code: 79903
FDA Application Number: part352 What is the FDA Application Number?
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.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/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.

Start Marketing Date: 05-20-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Spf Moisturizer Product Label Images

Spf Moisturizer Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Avobenzone 3%Octisalate 5.0%Octocrylene 5.0%

Purpose

Sunscreen

Use

  • Helps prevent sunburnif 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 the 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.

Directions

  • Apply liberally 15 minures before sun exposurereapply:after 80 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hoursSun Protecton Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decreade this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures includinglimit time in the sun, especiually from 10 a.m. - 2 p.m.wear long-sleeved shirts, pants, hats and sunglasseschilden under 6 months of age: Ask a doctor

Inactive Ingredients

Water, C12-15 alkyl benzoate, cetearyl alcohol, glycerin, dimethicone, Glycine soja (soybean) seed extract, phenyl trimethicone, arachidyl alcohol, cetearyl glucoside, chlorphenesin, benzyl alcohol, panthenol, behenyl alcohol, steareth-2, fragrance, steareth-21, polymethyl methacrylate, polyacrylamide, arachidyl glucoside, disodium EDTA, C13-14 isoparaffin, laureth-7, silica, titanium dioxide, mica

Other Information

May stain or damage some fabrics or surfaces.

Adverse Reactions

Satisfaction guaranteed - For questions or comments please call 1-888-287-1915DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716*This product is not manufactred or distributed by Johnson & Johnson Consumer Inc., owner of the registered trademarks Aveeno Postively radiant Daily Moisturizer Sunscreen Broad Spectrum SPF 15.** Oxybenzone & Octinoxate- Free

* Please review the disclaimer below.