NDC 64539-008 Granex Foam Acne Treatment
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 64539-008?
What are the uses for Granex Foam Acne Treatment?
Which are Granex Foam 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 Granex Foam 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:
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- BIOTIN (UNII: 6SO6U10H04)
- PEG/PPG-20/6 DIMETHICONE (UNII: PWZ7N4UIKE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ALOE (UNII: V5VD430YW9)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- PANTHENOL (UNII: WV9CM0O67Z)
- GLYCYRRHIZIN (UNII: 6FO62043WK)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- ISOBUTANE (UNII: BXR49TP611)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPANEDIOL (UNII: 5965N8W85T)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ALCOHOL (UNII: 3K9958V90M)
- IRIS X GERMANICA NOTHOVAR. FLORENTINA ROOT (UNII: M30XO5X4XD)
- ZINC SULFATE (UNII: 89DS0H96TB)
- WATER (UNII: 059QF0KO0R)
- ARCTIUM MINUS ROOT (UNII: IS8QAQ61Q5)
- CITRUS X LIMON FRUIT OIL (UNII: 0HNC1J1YED)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM SULFITE (UNII: VTK01UQK3G)
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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".