NDC 83104-301 Arca Regeneration Head Spa
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 83104-301?
What are the uses for Arca Regeneration Head Spa?
Which are Arca Regeneration Head Spa 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 Arca Regeneration Head Spa 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MONARDA DIDYMA LEAF (UNII: JY15982UBB)
- MENTHA PIPERITA LEAF (UNII: A389O33LX6)
- CHAMOMILE (UNII: FGL3685T2X)
- ROSEMARY (UNII: IJ67X351P9)
- FREESIA ALBA WHOLE (UNII: SS55L6C3QQ)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- OAT (UNII: Z6J799EAJK)
- PPG-10 CAPRYLYL ETHER (UNII: B1ML6JO7Z2)
- CASTOR OIL (UNII: D5340Y2I9G)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
- PANTHENOL (UNII: WV9CM0O67Z)
- HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
- GELATIN (UNII: 2G86QN327L)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- CAMELLIA JAPONICA SEED OIL (UNII: U37N0S910T)
- HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- WATER (UNII: 059QF0KO0R)
- TRIMETHYL OCTADECYL AMMONIUM CHLORIDE (UNII: CZ70647U92)
- LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- ALLANTOIN (UNII: 344S277G0Z)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
* 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".