NDC 49035-941 Daily Moisturizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49035 - Wal-mart Stores, Inc.,
- 49035-941 - Daily Moisturizer
Product Packages
NDC Code 49035-941-26
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 118 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 49035-941?
What are the uses for Daily Moisturizer?
Which are Daily Moisturizer 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 Daily Moisturizer 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:
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- DOCOSANOL (UNII: 9G1OE216XY)
- BIS-PHENYLPROPYL DIMETHICONE (15 CST) (UNII: 4836494CFT)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)
- GLYCERIN (UNII: PDC6A3C0OX)
- SOYBEAN (UNII: L7HT8F1ZOD)
- ISOCETETH-20 (UNII: O020065R7Z)
- LAURETH-7 (UNII: Z95S6G8201)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- PPG-10 CETYL ETHER (UNII: Q056X4917J)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Daily Moisturizer?
- RxCUI: 248684 - salicylic acid 0.5 % Topical Cream
- RxCUI: 248684 - salicylic acid 5 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".