NDC 69842-128 Cvs Health Maximum Strength Feminine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69842 - Cvs Pharmacy
- 69842-128 - Cvs Health Maximum Strength Feminine
Product Packages
NDC Code 69842-128-20
Package Description: 20 CLOTH in 1 POUCH
Product Details
What is NDC 69842-128?
What are the uses for Cvs Health Maximum Strength Feminine?
Which are Cvs Health Maximum Strength Feminine 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 Health Maximum Strength Feminine 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)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM (UNII: 9NEZ333N27)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Cvs Health Maximum Strength Feminine?
- 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".