NDC 59779-248 Cvs Extra Strength Itch Relief

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  3. NDC: 59779-248 Cvs Extra Strength Itch Relief

NDC Product Code 59779-248

NDC CODE: 59779-248

Proprietary Name: Cvs Extra Strength Itch Relief 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This product is used as usestemporarily relieves itching and pain associated with minor irritations, burns,scrapes, cuts, insect bites and rashes due to poison ivy, poison oak and poisonsumac. dries the oozing and weeping of poison ivy, poison oak and poison sumac.

NDC Code Structure

NDC 59779-248-25

Package Description: 59 mL in 1 BOTTLE, SPRAY

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

NDC Product Information

Cvs Extra Strength Itch Relief with NDC 59779-248 is product labeled by Cvs Pharmacy. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:


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)
  • ALCOHOL (UNII: 3K9958V90M)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • POVIDONE (UNII: FZ989GH94E)
  • TROMETHAMINE (UNII: 023C2WHX2V)

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: 08-10-2011 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

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

Why is diphenhydramine medication prescribed?
Diphenhydramine is used to relieve red, irritated, itchy, watery eyes; sneezing; and runny nose caused by hay fever, allergies, or the common cold. Diphenhydramine is als...
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Cvs Extra Strength Itch Relief Product Label Images

Cvs Extra Strength Itch 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                                                               PurposeDiphenhydramine HCL 2% ...................................................................Topical analgesicZinc Acetate 0.1%...............................................................................Skin Protectant

Otc - Purpose

UsesTemporarily relieves itching and pain associated with minor irritations, burns,scrapes, cuts, insect bites and rashes due to poison ivy, poison oak and poisonsumac. Dries the oozing and weeping of poison ivy, poison oak and poison 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

UsesTemporarily relieves itching and pain associated with minor irritations, burns,scrapes, cuts, insect bites and rashes due to poison ivy, poison oak and poisonsumac. Dries the oozing and weeping of poison ivy, poison oak and poison sumac.

Warnings

Warnings For external use only. Flammable. keep away from fire or flame.Do not use -  with any other product containing diphenhydramine, even one taken by mouth. - On large areas of the bodyAsk a doctor before use - on chicken pox - on measlesWhen using this product avoid contact with the eyesStop 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 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- do not use more than directed- Adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily- Children under 2 years of age: consult a doctorOther informationStore at 20 degrees to 25 degrees C (68 degrees to 77 degrees F)

Inactive Ingredient

Inactive Ingredientspurified water, SD alcohol 40-B, glycerin, povidone, tromethamine

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