NDC 59779-993 Cvs Pharmacy Maximum Strength Feminine Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs Pharmacy
- 59779-993 - Cvs Pharmacy
Product Packages
NDC Code 59779-993-01
Package Description: 89 g in 1 PACKAGE
Product Details
What is NDC 59779-993?
What are the uses for Cvs Pharmacy Maximum Strength Feminine Wipes?
Which are Cvs Pharmacy Maximum Strength Feminine Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5)
- PRAMOXINE (UNII: 068X84E056) (Active Moiety)
Which are Cvs Pharmacy Maximum Strength Feminine Wipes Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
What is the NDC to RxNorm Crosswalk for Cvs Pharmacy Maximum Strength Feminine Wipes?
- RxCUI: 1039541 - pramoxine HCl 1 % Medicated Pad
- RxCUI: 1039541 - pramoxine hydrochloride 10 MG/ML Medicated Pad
- RxCUI: 1039541 - pramoxine hydrochloride 1 % Medicated Pad
- RxCUI: 1039541 - pramoxine hydrochloride 1 % Medicated Wipe
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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".