NDC 69541-001 Asd 3-in-1
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What is NDC 69541-001?
What are the uses for Asd 3-in-1?
Which are Asd 3-in-1 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 Asd 3-in-1 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)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- JOJOBA OIL (UNII: 724GKU717M)
- NIACINAMIDE (UNII: 25X51I8RD4)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- GLYCERYL LAURATE (UNII: Y98611C087)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PANTHENOL (UNII: WV9CM0O67Z)
- WITCH HAZEL (UNII: 101I4J0U34)
- TOCOPHEROL (UNII: R0ZB2556P8)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SQUALANE (UNII: GW89575KF9)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
What is the NDC to RxNorm Crosswalk for Asd 3-in-1?
- RxCUI: 346298 - salicylic acid 2 % Topical Gel
- RxCUI: 346298 - salicylic acid 0.02 MG/MG Topical Gel
* Please review the disclaimer below.
[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".