NDC 73110-105 Smart Release Bpo 10 Percent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73110 - Skinclinical Ai, Llc
- 73110-105 - Smart Release Bpo
Product Packages
NDC Code 73110-105-11
Package Description: 30 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 73110-105?
What are the uses for Smart Release Bpo 10 Percent?
Which are Smart Release Bpo 10 Percent UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
Which are Smart Release Bpo 10 Percent 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- PEG-8/SMDI COPOLYMER (UNII: CCX72L6NY6)
- LACTOBACILLUS REUTERI (UNII: 9913I24QEE)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- LACTIC ACID (UNII: 33X04XA5AT)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- ZINC SULFATE (UNII: 89DS0H96TB)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- GRAPEFRUIT OIL (UNII: YR377U58W9)
- ORANGE OIL (UNII: AKN3KSD11B)
- TANGERINE PEEL (UNII: JU3D414057)
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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".