NDC 59779-622 Cvs Capsaicin

  1. Labeler Index
  2. Cvs Pharmacy
  3. NDC: 59779-622 Cvs Capsaicin

NDC Product Code 59779-622

NDC CODE: 59779-622

Proprietary Name: Cvs Capsaicin 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 59779-622-65

Package Description: 1 TUBE in 1 CARTON > 42.5 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 Capsaicin with NDC 59779-622 is a product labeled by Cvs Pharmacy. The generic name of Cvs Capsaicin is . The product's dosage form is and is administered via form.

Labeler Name: Cvs Pharmacy

Dosage Form: -

Product Type: 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.

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.
  • DIGLYCOL STEARATE (UNII: 94YQ11Y95F)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • SORBITOL (UNII: 506T60A25R)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • WATER (UNII: 059QF0KO0R)

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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Cvs Capsaicin Product Label Images

Cvs Capsaicin 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                                 PurposeCapsaicin 0.1%............................................Topical analgesic

Otc - Purpose

Uses for the temporary relieves of minor aches and pains of muscles and joints associated with:- arthritis - simple backache - strains - bruises

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If case of overdose or allergic reaction, seek medical attention or contacta Poison Control Center right away.

Indications & Usage

Uses for the temporary relieves of minor aches and pains of muscles and joints associated with:
- arthritis - simple backache - strains - bruises

Warnings

Warnings For external use onlyWhen using this product- use only as directed - do not apply to wounds, damaged, broken or irritated skin - avoid contactwith the eyes or mucous membranes - a slight burning sensation may occur upon application, butgenerally disappears in several days - if severe burning occurs, discontinue use - do not exposethe treated area to heat or direct sunlight - do not bandage - do not use with heating padStop use and consult a dentist or doctor if: -  condition worsens - symptoms persist for more than 7 days or clear up and occur again within a few days- redness is present - irritation develops Keep out of the reach of children.In case of overdose or allergic reaction, seek medical attention or contact a Poison Control Center right away.If pregnant or breast feeding, ask a health professional before use.

Dosage & Administration

Directions  Adults and children over 18 years- apply to affected area- Massage into the painful area until thoroughly absorbed- Repeat as necessary, but no more than 3 to 4 times daily- WASH HANDS WITH SOAP AND WATER AFTER APPLYINGChildren 18 years and younger: ask a doctor.

Inactive Ingredient

Inactive Ingredientspurified water, petrolatum, cetyl alcohol glyceryl stearate, PEG-40 stearate, isopropyl myristate, sorbitol, PEG-2 stearate, benzyl alcohol

* Please review the disclaimer below.