NDC 0363-8222 Sensitive Skin 3 Oz
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0363 - Walgreen Company
- 0363-8222 - Sensitive Skin 3 Oz
Product Packages
NDC Code 0363-8222-81
Package Description: 88.7 mL in 1 BOTTLE
Product Details
What is NDC 0363-8222?
What are the uses for Sensitive Skin 3 Oz?
Which are Sensitive Skin 3 Oz UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Sensitive Skin 3 Oz 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)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
- CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
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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".