NDC 80377-012 Acne Control Essence
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80377 - Shenzhen Rongchuang Zhiyuan Industrial Co., Ltd.
- 80377-012 - Acne Control Essence
Product Packages
NDC Code 80377-012-01
Package Description: 50 g in 1 BOTTLE
Product Details
What is NDC 80377-012?
Which are Acne Control Essence UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ) (Active Moiety)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Acne Control Essence 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:
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MELIA AZEDARACH LEAF (UNII: 8194E3H7D4)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
* 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".