NDC 61369-101 Klenskin Showeron Sunscreen Spf-30
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 61369-101?
What are the uses for Klenskin Showeron Sunscreen Spf-30?
Which are Klenskin Showeron Sunscreen Spf-30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Klenskin Showeron Sunscreen Spf-30 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYQUATERNIUM-10 (125 MPA.S AT 2%) (UNII: L45WU8S981)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- HYDROLYZED ELASTIN, BOVINE, ALKALINE (1000 MW) (UNII: ZR28QKN0WT)
- SHEANUT OIL (UNII: O88E196QRF)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- ETHYLENEDIAMINE (UNII: 60V9STC53F)
- DIISOSTEARYL DIMER DILINOLEATE (UNII: 04P17590AP)
- HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- EDETATE SODIUM (UNII: MP1J8420LU)
- HYDROXYETHYL LAURDIMONIUM CHLORIDE (UNII: 8467K53E3Y)
- GELLAN GUM (LOW ACYL) (UNII: 7593U09I4D)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
- CAMELLIA OLEIFERA SEED (UNII: 59ED29FM2J)
- POMEGRANATE SEED OIL (UNII: 0UI45XV0T6)
- RASPBERRY SEED OIL (UNII: 9S8867952A)
- CRANBERRY SEED OIL (UNII: 73KDS3BW5E)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- CARRAGEENAN (UNII: 5C69YCD2YJ)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
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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".