NDC 72192-022 Unicorn Snot 30 Glitter Sunscreen Space Junk
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72192 - Jailbreak Toys, Inc.
- 72192-022 - Unicorn Snot 30
Product Characteristics
Product Packages
NDC Code 72192-022-05
Package Description: 148 mL in 1 TUBE
Product Details
What is NDC 72192-022?
What are the uses for Unicorn Snot 30 Glitter Sunscreen Space Junk?
Which are Unicorn Snot 30 Glitter Sunscreen Space Junk UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
Which are Unicorn Snot 30 Glitter Sunscreen Space Junk 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:
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- POLYESTER-7 (UNII: 0841698D2F)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- REGENERATED CELLULOSE (UNII: BX81F82EWG)
- SAGE OIL (UNII: U27K0H1H2O)
- SORBITAN MONOPALMITATE (UNII: 77K6Z421KU)
- STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- PROPANEDIOL (UNII: 5965N8W85T)
- UREA (UNII: 8W8T17847W)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- ORANGE OIL (UNII: AKN3KSD11B)
- ETHYL FERULATE (UNII: 5B8915UELW)
- MICA (UNII: V8A1AW0880)
- GRAPEFRUIT (UNII: O82C39RR8C)
- CITRUS RETICULATA LEAF OIL (UNII: 1515UE78IH)
- GLYCERIN (UNII: PDC6A3C0OX)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALUMINUM (UNII: CPD4NFA903)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- WATER (UNII: 059QF0KO0R)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETIC ACID (UNII: 9G34HU7RV0)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
* 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".