NDC 59779-811 Cvs Deep Cleansing Astringent

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  3. NDC: 59779-811 Cvs Deep Cleansing Astringent

NDC Product Code 59779-811

NDC CODE: 59779-811

Proprietary Name: Cvs Deep Cleansing Astringent 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

  • 59779 - Cvs Pharmacy

NDC 59779-811-31

Package Description: 250 mL in 1 BOTTLE, PLASTIC

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

NDC Product Information

Cvs Deep Cleansing Astringent with NDC 59779-811 is a product labeled by Cvs Pharmacy. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 199308.

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)
  • ALCOHOL (UNII: 3K9958V90M)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • BENZOPHENONE (UNII: 701M4TTV9O)
  • DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
  • LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ISOCETYL ALCOHOL (UNII: 1800H64066)
  • PEG-32 STEARATE (UNII: 33GX5WQC0M)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • SODIUM CITRATE (UNII: 1Q73Q2JULR)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Product Labeler Information

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

Labeler Name: Cvs Pharmacy
Labeler Code: 59779
Start Marketing Date: 07-08-2010 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: 12-31-2017 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".

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Information for Patients

Salicylic Acid Topical

Salicylic Acid Topical is pronounced as (sal'' i sil' ik as' id)

Why is salicylic acid topical medication prescribed?
Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions ...
[Read More]

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Cvs Deep Cleansing Astringent Product Label Images

Cvs Deep Cleansing Astringent 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

Otc - Active Ingredient

Active ingredient                                 PurposeSalicylic Acid 0.5%.........................................Acne medication

Otc - Purpose

Uses for the treatment of acne

Otc - Keep Out Of Reach Of Children

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

Indications & Usage

Uses for the treatment of acne

Warnings

Warnings For external use onlyFlammable, Keep away from fire or flameWhen using this product- avoid contact with eyes. If contact occurs, flush thoroughly with water.- using other topical acne medications at the same time or right after use of this product, may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

Directions- cleanse skin thoroughly before applying medication- moisten cotton ball or pad and pat over face and neck- because too much drying of the skin may occur, start with 1 application daily, then gradually increase to 2 to 3 times daily if needed or as directed by a doctor- if bothersome dryness or peeling occurs, reduce application to once a day or every other dayOther information store at room temperature

Inactive Ingredient

Inactive Ingredientsalcohol, alge extract, aloe barbadensis leaf extract, benzophenone-4, blue-1, dentatonium benzonate, dimethicone propyl PG-betaine, fragrance, glycerin, isoceteth-20, PEG-32, propylene glycol, purified water, sodium citrate

* Please review the disclaimer below.