NDC 63868-947 Quality Choice Extra Strength Anti Itch

NDC Product Code 63868-947

NDC CODE: 63868-947

Proprietary Name: Quality Choice Extra Strength 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.

NDC Code Structure

  • 63868 - Chain Drug Marketing Association Inc
    • 63868-947 - Quality Choice Extra Strength Anti Itch

NDC 63868-947-30

Package Description: 1 TUBE in 1 CARTON > 30 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

Quality Choice Extra Strength Anti Itch with NDC 63868-947 is a product labeled by Chain Drug Marketing Association Inc. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1087026.

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)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Chain Drug Marketing Association Inc
Labeler Code: 63868
Start Marketing Date: 02-13-2012 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".

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Information for Patients

Diphenhydramine Topical

Diphenhydramine Topical is pronounced as (dye fen hye' dra meen)

Why is diphenhydramine topical medication prescribed?
Diphenhydramine, an antihistamine, is used to relieve the itching of insect bites, sunburns, bee stings, poison ivy, poison oak, and minor skin irritation.This medication...
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Quality Choice Extra Strength Anti Itch Product Label Images

Quality Choice Extra Strength 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 Ingredients                                                                               PurposeDiphenhydramine hydrochloride USP, 2%.............................................AntihistamineZinc acetate, 0.1%.............................................................................Skin protectant

Otc - Purpose

  • Usesfor the temporary relief of itching and pain associated with minor skin irritations and rashes due to insect bites, poison ivy, poison oak, and poison sumacdries the oozing and weeping of poison ivy, poison oak and poison sumac


WarningsFor external use only

Otc - Do Not Use

  • Do not use on chicken pox, measles, sunburn, oozing skin, broken blisters or on extensive areas of the skin more than directedany other drug containing diphenhydramine while using this product

Otc - When Using

When using this product avoid contact with the eyes

Otc - Stop Use

Stop use and ask a doctor if condition worsens, or if symptoms persists for more than 7 days, or clear up and occur again within a few days

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

  • Directionsadults and children 12 years of age and older,apply to affected area not more than 3 to 4 times daily, or as directed by a doctorchildren under 12 years of age, consult a doctor

Storage And Handling

  • Other informationstore at room temperatureLot No. and Exp. Date: see box or see crimp of tube

Inactive Ingredient

Inactive ingredientsglycerin, sodium chloride, petrolatum, cetyl alcohol, dimethicone, isopropyl palmitate, distearyldimodium chloride (1-Octadecanaminium, N, N-Dimmethyl-N-Octadecyl-Chloride), methylparaben, propylparaben, purified water, hydroxyethyl cellulose

Dosage & Administration


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