NDC 59779-078 Salicylic Acid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs
- 59779-078 - Salicylic Acid
Product Packages
NDC Code 59779-078-08
Package Description: 120 mL in 1 BOTTLE
Product Details
What is NDC 59779-078?
What are the uses for Salicylic Acid?
Which are Salicylic Acid 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 Salicylic Acid 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)
- DICAPRYLYL ETHER (UNII: 77JZM5516Z)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- MENTHYL LACTATE (UNII: 2BF9E65L7I)
- STEARETH-20 (UNII: L0Q8IK9E08)
- XANTHAN GUM (UNII: TTV12P4NEE)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
What is the NDC to RxNorm Crosswalk for Salicylic Acid?
- 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".