NDC 69423-360 Olay Total Effects Whip Active Moisturizer Broad Spectrum Spf 40 Sunscreen

Avobenzone, Homosalate, Octisalate, Octocrylene, And Oxybenzone

NDC Product Code 69423-360

NDC Code: 69423-360

Proprietary Name: Olay Total Effects Whip Active Moisturizer Broad Spectrum Spf 40 Sunscreen What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Avobenzone, Homosalate, Octisalate, Octocrylene, And Oxybenzone What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 69423 - The Procter & Gamble Manufacturing Company
    • 69423-360 - Olay Total Effects Whip Active Moisturizer Broad Spectrum Spf 40 Sunscreen

NDC 69423-360-48

Package Description: 1 JAR in 1 CARTON > 48 g in 1 JAR

NDC Product Information

Olay Total Effects Whip Active Moisturizer Broad Spectrum Spf 40 Sunscreen with NDC 69423-360 is a a human over the counter drug product labeled by The Procter & Gamble Manufacturing Company. The generic name of Olay Total Effects Whip Active Moisturizer Broad Spectrum Spf 40 Sunscreen is avobenzone, homosalate, octisalate, octocrylene, and oxybenzone. The product's dosage form is cream and is administered via topical form.

Labeler Name: The Procter & Gamble Manufacturing Company

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Olay Total Effects Whip Active Moisturizer Broad Spectrum Spf 40 Sunscreen 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 g/100g
  • HOMOSALATE 10 g/100g
  • OCTISALATE 5 g/100g
  • OCTOCRYLENE 9 g/100g

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.

  • STARCH, TAPIOCA (UNII: 24SC3U704I)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • NIACINAMIDE (UNII: 25X51I8RD4)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • PANTHENOL (UNII: WV9CM0O67Z)
  • CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • DOCOSANOL (UNII: 9G1OE216XY)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • PALMITIC ACID (UNII: 2V16EO95H1)
  • POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
  • ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
  • GREEN TEA LEAF (UNII: W2ZU1RY8B0)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • DIMETHICONOL GUM (UNII: 4MJ9GU3T1P)

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: The Procter & Gamble Manufacturing Company
Labeler Code: 69423
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: 09-01-2019 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: 12-31-2020 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Olay Total Effects Whip Active Moisturizer Broad Spectrum Spf 40 Sunscreen Product Label Images

Olay Total Effects Whip Active Moisturizer Broad Spectrum Spf 40 Sunscreen 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

Other

Drug Facts

Distr. by PROCTER & GAMBLE,







CINCINNATI, OH 45202

Otc - Active Ingredient

Avobenzone 3.0%Homosalate 10.0%Octisalate 5.0%Octocrylene 9.0%

Otc - Purpose

Sunscreen

Uses

  • 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

For external use only

Otc - Do Not Use

Do not use on damaged or broken skin

Otc - When Using

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

Otc - Stop Use

Stop use and ask a doctor if rash occurs

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Apply liberally 15 minutes before sun exposurereapply at least every 2 hoursuse water resistant sunscreen if swimming or sweatingSun 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 sun, especially from 10 a.m. – 2 p.m.wear long-sleeved shirts, pants, hats, and sunglasseschildren under 6 months: ask a doctor

Other Information

  • Protect this product from excessive heat and direct sun

Inactive Ingredients

Water, tapioca starch, glycerin, niacinamide*, dimethicone, panthenol**, tocopheryl acetate***, sodium ascorbyl phosphate^, camellia sinensis leaf extract^^, sodium polyacrylate starch, stearyl alcohol, caprylyl glycol, behenyl alcohol, 1,2-hexanediol, phenoxyethanol, cetyl alcohol, dimethiconol, PEG-100 stearate, fragrance, polymethylsilsesquioxane, cetearyl glucoside, cetearyl alcohol, BHT, disodium EDTA, stearic acid, palmitic acid.*Vitamin B3, **Pro-Vitamin B5, ***Vitamin E, ^Vitamin C, ^^Green Tea

* Please review the disclaimer below.