NDC 59779-621 Cvs Medicated Anti-itch

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  2. Cvs Pharmacy
  3. NDC: 59779-621 Cvs Medicated Anti-itch

NDC Product Code 59779-621

NDC CODE: 59779-621

Proprietary Name: Cvs Medicated Anti-itch 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This product is used as usesfor the temporary relief of pain and discomfort cause by- minor burns - sunburn - scrapes - insect bites- minor skin irritations - rashes due to poison ivy, oak and sumac

NDC Code Structure

NDC 59779-621-64

Package Description: 1 TUBE in 1 CARTON > 56 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

Cvs Medicated Anti-itch with NDC 59779-621 is product labeled by Cvs Pharmacy. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:


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)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • TRIDECETH-6 (UNII: 3T5PCR2H0C)
  • STEARETH-21 (UNII: 53J3F32P58)
  • STEARETH-2 (UNII: V56DFE46J5)
  • THYMOL (UNII: 3J50XA376E)
  • ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
  • METHYL SALICYLATE (UNII: LAV5U5022Y)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • EUCALYPTUS OIL (UNII: 2R04ONI662)

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".

* Please review the disclaimer below.

Cvs Medicated Anti-itch Product Label Images

Cvs Medicated Anti-itch 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                                 PurposeMenthol 1%....................................................Anti-Itch Pain ReliefPramoxine Hydrochloride 1%............................Anti-Itch Pain Relief

Otc - Purpose

UsesFor the temporary relief of pain and discomfort cause by- minor burns - sunburn - scrapes - insect bites- minor skin irritations - rashes due to poison ivy, oak and sumac

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.

Indications & Usage

UsesFor the temporary relief of pain and discomfort cause by
- minor burns - sunburn - scrapes - insect bites
- minor skin irritations - rashes due to poison ivy, oak and sumac

Warnings

Warnings For external use onlyDo Not use - under bandages or compresses When using this product- avoid contact with the eyesStop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

Directions- Adults and children 2 years and older: apply to affected area not more than 2 tim- Children under 2 years of age: do not use, consult a doctor

Inactive Ingredient

Inactive IngredientsWater, Propylene Glycol, Petrolatum, Stearyl Alcohol, Aloe Barbadensis Gel, Sodium Acrylates Copolymer, Mineral Oil, Steareth 21, PPG 1 Trideceth, 6, Toco[heryl Acetate, Disodium EDTA, Methyl Salicylate, Thymol, Eucalyptol, Triethanolamine, Iodopropynyl Butylcarbamate, Diozolidinyl Urea

* Please review the disclaimer below.