NDC 59779-620 Cvs Extra Strength Pain Relief

NDC Product Code 59779-620

NDC 59779-620-35

Package Description: 99.2 g in 1 JAR

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

NDC Product Information

Cvs Extra Strength Pain Relief with NDC 59779-620 is a product labeled by Cvs Pharmacy. The generic name of Cvs Extra Strength Pain Relief 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.

  • PARAFFIN (UNII: I9O0E3H2ZE)
  • PETROLATUM (UNII: 4T6H12BN9U)

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: 07-10-2010 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 Extra Strength Pain Relief Product Label Images

Cvs Extra Strength Pain Relief 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 7.6%...................................................Topical AnalgesicMethyl Salicylate 29%.......................................Topical Analgesic

Otc - Purpose

Uses temporary relieves minor pain associated with: - arthritis - simple backache - muscle strains- muscle sprains - bruises - cramps

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

Uses temporary relieves minor pain associated with:
- arthritis - simple backache - muscle strains
- muscle sprains - bruises - cramps

Warnings

Warnings For external use onlyAllergy alert:  if prone to allergic reaction from aspirin or salicylates, consult a doctor before use.When using this product - use only as directed - avoid contact with the eyes or mucous membranes- do not bandage tightly or use with a heating pad - do not apply to wounds or damaged skinAsk a doctor before use if - condition worsens - redness is present - irritation develops - symptoms persist for more than 7 days or clear up and occur again within a few days. If pregnant or breast-feeding, ask a health professional before use.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 12 years of age and older:- apply generously to affected area- massage into painful area until thoroughly absorbed into skin- repeat as necessary, but no more than 4 times dilychildren under 12 years of age: consult a doctor

Inactive Ingredient

Inactive Ingredients parrafin, petrolatum

* Please review the disclaimer below.