NDC 11822-4591 Renewal Anti-wrinkle

  1. Labeler Index
  2. Rite Aid Corporation
  3. NDC: 11822-4591 Renewal Anti-wrinkle

NDC Product Code 11822-4591

NDC CODE: 11822-4591

Proprietary Name: Renewal Anti-wrinkle 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.

NDC Code Structure

  • 11822 - Rite Aid Corporation

NDC 11822-4591-1

Package Description: 1 TUBE in 1 CARTON > 40 g in 1 TUBE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Renewal Anti-wrinkle with NDC 11822-4591 is a product labeled by Rite Aid Corporation. The product's dosage form is and is administered via form.

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • DOCOSANOL (UNII: 9G1OE216XY)
  • SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • PANTHENOL (UNII: WV9CM0O67Z)
  • DMDM HYDANTOIN (UNII: BYR0546TOW)
  • CHAMOMILE (UNII: FGL3685T2X)
  • VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Product Labeler Information

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

Labeler Name: Rite Aid Corporation
Labeler Code: 11822
Start Marketing Date: 08-01-2012 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: 12-31-2019 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Renewal Anti-wrinkle Product Label Images

Renewal Anti-wrinkle 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 Ingredient

Avobenzone 3.0%Octocrylene 10.0%

Purpose

Sunscreen

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

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.

Directions

  • •Apply liberally 15 minutes before sun exposure. •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 other sun protection measures including: •limit time in the sun, especially from 10 a.m. - 2 p.m. •wear long-sleeved shirts, pants, hats and sunglasses

Other Information

  • •protect the product in this container from excessive heat and direct sun

Inactive Ingredients

Water, C12-15 alkyl benzoate, glycerin, cyclopentasiloxane, cetyl alcohol, polyglyceryl-10 pentastearate, behenyl alcohol, sodium steroyl lactylate, cetearyl alcohol, cetearyl glucoside, butylene glycol, titanium dioxide, alumina, simethicone, potassium cetyl phosphate, propylene glycol, diazolidinyl urea, methylparaben, propyleparaben, tocopheryl acetate (vitamin E), panthenol (pro-vitamin B5), DMDM hydantoin, dimethicone, chamomilla recutita (matricaria) flower extract, retinyl palmitate, disodium EDTA, triethanolamine, BHT

* Please review the disclaimer below.