NDC 73110-103 Smart Release Mandelic 8 Percent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73110 - Skinclinical Ai, Llc
- 73110-103 - Smart Release Mandelic
Product Packages
NDC Code 73110-103-11
Package Description: 30 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 73110-103?
What are the uses for Smart Release Mandelic 8 Percent?
Which are Smart Release Mandelic 8 Percent 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 Smart Release Mandelic 8 Percent 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)
- ALCOHOL (UNII: 3K9958V90M)
- MANDELIC ACID (UNII: NH496X0UJX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- WITCH HAZEL (UNII: 101I4J0U34)
- LACTOBACILLUS REUTERI (UNII: 9913I24QEE)
- PEG-8/SMDI COPOLYMER (UNII: CCX72L6NY6)
- NIACINAMIDE (UNII: 25X51I8RD4)
- LACTIC ACID (UNII: 33X04XA5AT)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- ZINC SULFATE (UNII: 89DS0H96TB)
- GLYCERIN (UNII: PDC6A3C0OX)
- OPUNTIA FICUS-INDICA (UNII: 23Z87HTQ6P)
- YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U)
- HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
- BILBERRY (UNII: 9P2U39H18W)
- SACCHARUM OFFICINARUM WHOLE (UNII: 3Z20C92XNB)
- ORANGE (UNII: 5EVU04N5QU)
- LEMON (UNII: 24RS0A988O)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- CITRUS MAXIMA FRUIT RIND OIL (UNII: 8U3877WD44)
- ORANGE OIL (UNII: AKN3KSD11B)
- MANDARIN OIL (UNII: NJO720F72R)
What is the NDC to RxNorm Crosswalk for Smart Release Mandelic 8 Percent?
- RxCUI: 252296 - salicylic acid 0.5 % Topical Gel
- RxCUI: 252296 - salicylic acid 0.005 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".