NDC 65734-740 Advance Acne Care
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65734 - Swabplus Inc.
- 65734-740 - Advance Acne Care
Product Packages
NDC Code 65734-740-00
Package Description: 1 KIT in 1 CARTON * 24 APPLICATOR in 1 PACKAGE (65734-741-24) / .15 mL in 1 APPLICATOR (65734-741-00) * 24 APPLICATOR in 1 PACKAGE (65734-742-24) / .15 mL in 1 APPLICATOR (65734-742-00)
Product Details
What is NDC 65734-740?
What are the uses for Advance Acne Care?
Which are Advance Acne Care UNII Codes?
The UNII codes for the active ingredients in this product are:
- SILVER (UNII: 3M4G523W1G)
- SILVER (UNII: 3M4G523W1G) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Advance Acne Care 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:
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- WATER (UNII: 059QF0KO0R)
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- ISOCETETH-20 (UNII: O020065R7Z)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM (UNII: 9NEZ333N27)
- SORBITAN (UNII: 6O92ICV9RU)
- WITCH HAZEL (UNII: 101I4J0U34)
What is the NDC to RxNorm Crosswalk for Advance Acne Care?
- RxCUI: 797892 - salicylic acid 2 % Medicated Pad
- RxCUI: 797892 - salicylic acid 20 MG/ML Medicated Pad
- RxCUI: 797892 - salicylic acid 2 % Topical Swab
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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".