NDC 68479-313 Breakout Clearing Overnight Treatment
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 68479-313?
What are the uses for Breakout Clearing Overnight Treatment?
Which are Breakout Clearing Overnight Treatment 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 Breakout Clearing Overnight Treatment 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)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TEA TREE OIL (UNII: VIF565UC2G)
- FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- PORPHYRA UMBILICALIS (UNII: 14AN0J70WO)
- CUCUMBER (UNII: YY7C30VXJT)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ZINC ACETATE (UNII: FM5526K07A)
- PROPANEDIOL (UNII: 5965N8W85T)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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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".