NDC 69842-842 Itch Relief Medicated Pads Cvs

NDC Product Code 69842-842

NDC CODE: 69842-842

Proprietary Name: Itch Relief Medicated Pads Cvs 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

  • 69842 - Cvs

NDC 69842-842-03

Package Description: 69 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

Itch Relief Medicated Pads Cvs with NDC 69842-842 is a product labeled by Cvs. The product's dosage form is and is administered via form.

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.

  • ALCOHOL (UNII: 3K9958V90M)
  • OATMEAL (UNII: 8PI54V663Y)
  • CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • POLYSORBATE 40 (UNII: STI11B5A2X)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • SODIUM CITRATE (UNII: 1Q73Q2JULR)
  • 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
Labeler Code: 69842
Start Marketing Date: 03-15-2017 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: 12-31-2019 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.

Itch Relief Medicated Pads Cvs Product Label Images

Itch Relief Medicated Pads Cvs 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

Active Ingredient

Pramoxine  HCl 1%               External AnalgesicZinc Acetate 0.1%                 Skin Pretectant

Uses

  • Temporarily relieves pain and itching asociated with: rashes due to poison ivy, poison oak or poison sumac.insect bites.minor skin irritation.minor cuts. dries the oozing and weeping of poison ivy, poison oak and poison sumac.

Warnings

For external use only.Flammable: Do not use near heat, flame, or while smoking.​​​

When Using This Product

  • Keep out of eyes. Rinse with water to remove.

Stop Use And Ask A Doctor If

  • Condition worsens or does not improve within 7 days.symptoms persist for more than 7 days or clear up and occur again with in a few days.

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily.children under 2 years of age: ask a doctor.

Inactive Ingredients

Avena Sativa (Oat) Meal ExtractCamphorCitric AcidDiazolidinyl UreaFragranceGlycerinHydroxypropyl MethylcelluloseMethylparabenPolysorbate 40Propylene GlycolPropylparabenSD Alcohol 38-BSodium CitrateWater

* Please review the disclaimer below.