NDC 69842-674 Maximum Strength Acne Spot Treatment Cvs Health
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69842 - Cvs
- 69842-674 - Maximum Strength Acne Spot Treatment
Product Packages
NDC Code 69842-674-01
Package Description: 28 g in 1 TUBE
Product Details
What is NDC 69842-674?
Which are Maximum Strength Acne Spot Treatment Cvs Health UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
Which are Maximum Strength Acne Spot Treatment Cvs Health 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:
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- BENTONITE (UNII: A3N5ZCN45C)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Maximum Strength Acne Spot Treatment Cvs Health?
- RxCUI: 106315 - benzoyl peroxide 10 % Topical Cream
- RxCUI: 106315 - benzoyl peroxide 100 MG/ML Topical Cream
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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".