NDC 65923-587 Family Care Ultra Acne Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65923 - United Exchange Corp.
- 65923-587 - Family Care Ultra Acne Treatment
Product Packages
NDC Code 65923-587-12
Package Description: 1 PACKAGE in 1 BOX / 11.9 g in 1 PACKAGE
Product Details
What is NDC 65923-587?
What are the uses for Family Care Ultra Acne Treatment?
Which are Family Care Ultra Acne Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Family Care Ultra Acne Treatment 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITOL (UNII: 506T60A25R)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HELICHRYSUM ITALICUM FLOWER (UNII: P62Y550X24)
- MENTHOL (UNII: L7T10EIP3A)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Family Care Ultra Acne Treatment?
- RxCUI: 346298 - salicylic acid 2 % Topical Gel
- RxCUI: 346298 - salicylic acid 0.02 MG/MG Topical Gel
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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".