NDC 59779-152 Cvs Pharmacy Clear Skin Daily Moisturizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs Pharmacy
- 59779-152 - Cvs Pharmacy
Product Packages
NDC Code 59779-152-04
Package Description: 118 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 59779-152?
What are the uses for Cvs Pharmacy Clear Skin Daily Moisturizer?
Which are Cvs Pharmacy Clear Skin 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 Cvs Pharmacy Clear Skin 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)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- BIS-PHENYLPROPYL DIMETHICONE (15 CST) (UNII: 4836494CFT)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- SOYBEAN (UNII: L7HT8F1ZOD)
- ISOCETETH-20 (UNII: O020065R7Z)
- LAURETH-7 (UNII: Z95S6G8201)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYACRYLAMIDE (1300000 MW) (UNII: SC5Y4X78TG)
- PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Cvs Pharmacy Clear Skin Daily Moisturizer?
- RxCUI: 199134 - salicylic acid 0.5 % Topical Lotion
- RxCUI: 199134 - salicylic acid 5 MG/ML Topical Lotion
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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".