NDC 76147-236 Strivectin Advanced Retinol Daily Repair Moisturizer Spf30

Avobenzone, Homosalate, Octisalate, Octocrylene

NDC Product Code 76147-236

NDC CODE: 76147-236

Proprietary Name: Strivectin Advanced Retinol Daily Repair Moisturizer Spf30 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 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

  • 76147 - Strivectin Operating Company, Inc.
    • 76147-236 - Strivectin Advanced Retinol Daily Repair Moisturizer

NDC 76147-236-50

Package Description: 1 TUBE in 1 BOX > 50 mL in 1 TUBE

NDC Product Information

Strivectin Advanced Retinol Daily Repair Moisturizer Spf30 with NDC 76147-236 is a a human over the counter drug product labeled by Strivectin Operating Company, Inc.. The generic name of Strivectin Advanced Retinol Daily Repair Moisturizer Spf30 is avobenzone, homosalate, octisalate, octocrylene. The product's dosage form is lotion and is administered via topical form.

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.

Strivectin Advanced Retinol Daily Repair Moisturizer Spf30 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.


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.

  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • ERYTHRITOL (UNII: RA96B954X6)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
  • METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
  • CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
  • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
  • WATER (UNII: 059QF0KO0R)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
  • MYRISTYL NICOTINATE (UNII: 8QWM6I035C)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4)
  • COCO GLUCOSIDE (UNII: ICS790225B)
  • POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
  • PRUNUS PERSICA FLOWER (UNII: 19GWB0JENH)
  • HEXAPEPTIDE-49 (UNII: 5UE28J54GV)
  • RETINOL (UNII: G2SH0XKK91)
  • YEAST .BETA.-D-GLUCAN (UNII: 44FQ49X6UN)
  • GINGER (UNII: C5529G5JPQ)
  • LEVOMENOL (UNII: 24WE03BX2T)
  • .BETA.-SITOSTEROL (UNII: S347WMO6M4)
  • HIBISCUS SABDARIFFA WHOLE (UNII: UH3Z91Y49Y)
  • RICE GERM (UNII: 7N2B70SFEZ)
  • SOYBEAN (UNII: L7HT8F1ZOD)
  • ORYZA SATIVA WHOLE (UNII: 84IVV0906Z)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • GLUCONOLACTONE (UNII: WQ29KQ9POT)
  • POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
  • SOYBEAN OIL (UNII: 241ATL177A)
  • ASCORBYL PALMITATE (UNII: QN83US2B0N)
  • ASCORBIC ACID (UNII: PQ6CK8PD0R)
  • ISOHEXADECANE (UNII: 918X1OUF1E)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • MICA (UNII: V8A1AW0880)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • SODIUM LACTATE (UNII: TU7HW0W0QT)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • BENZOIC ACID (UNII: 8SKN0B0MIM)
  • POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632)
  • SODIUM PHOSPHATE (UNII: SE337SVY37)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
  • .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
  • EUGENOL (UNII: 3T8H1794QW)
  • GERANIOL (UNII: L837108USY)
  • LINALOOL, (+/-)- (UNII: D81QY6I88E)
  • PENTYLENE GLYCOL (UNII: 50C1307PZG)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
  • PROPYL GALLATE (UNII: 8D4SNN7V92)
  • AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • SODIUM ACRYLATE (UNII: 7C98FKB43H)
  • 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
  • TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
  • ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)

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: Strivectin Operating Company, Inc.
Labeler Code: 76147
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: 10-31-2021 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.

Strivectin Advanced Retinol Daily Repair Moisturizer Spf30 Product Label Images

Strivectin Advanced Retinol Daily Repair Moisturizer Spf30 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 2.70%

Homosalate 6.30%

Octisalate 4.05%

Octocrylene 9.00%

Purpose

Sunscreen

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

Otc - Keep Out Of Reach Of Children

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

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

Other Information

Protect the product in this container from excessive heat and direct sun.

Directions

  • Apply generously 15 minutes before sun exposure and as neededReapply at least every two hours.Use a water resistant sunscreen if swimming or sweating.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. to 2 p.m.wear long-sleeved shirts, pants, hats, and sunglasses.Children under 6 months of age: Ask a doctor.

Inactive Ingredients

Aqua/Water/Eau, Propanediol, Isononyl Isononanoate, Myristyl Nicotinate, Glycerin, Cetearyl Alcohol, Ethylhexyl Isononanoate, Coco-Glucoside, Potassium Cetyl Phosphate, Prunus Persica (Peach) Flower Extract, Nicotiana Benthanmiana Hexapeptide-40 sh-Polypeptide-76, Retinol, Beta-Glucan, Zingiber Of­cinale (Ginger) Root Extract, Bisabolol, Beta-Sitosterol, Hibiscus Sabdariffa Fruit Extract, Oryza Sativa (Rice) Germ Extract, Glycine Soja (Soybean) Extract, Oryza Sativa (Rice) Extract, Dimethicone, Bacillus/Sea Salt Ferment Filtrate, Sodium Hyaluronate, Gluconolactone, Polyglyceryl-3 Diisostearate, Glycine Soja (Soybean) Oil, Ascorbyl Palmitate, Ascorbic Acid, Tocopheryl Acetate, Polysorbate 20, Erythritol, Glucose, Pentylene Glycol, Butylene Glycol, Methyl Methacrylate/Glycol Dimethacrylate Crosspolymer, Caprylyl Glycol, Sodium Acrylates Copolymer, Lecithin, 1,2-Hexanediol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tetrasodium Glutamate Diacetate, Caprylhydroxamic Acid, Polysilicone-11, Propyl Gallate, Parfum/Fragrance, Aminomethyl Propanol, Disodium EDTA, Xanthan Gum, Phenethyl Alcohol, Citric Acid, BHT, Sodium Benzoate, Potassium Sorbate, Alpha-Isomethyl Ionone

* Please review the disclaimer below.