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.
Non-Proprietary Name: 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

  • 59779 - Cvs Pharmacy

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 a product labeled by Cvs Pharmacy. The generic name of Cvs Medicated Anti-itch is . The product's dosage form is and is administered via form.

Labeler Name: Cvs Pharmacy

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.