NDC 68479-150 Super Sensitive Shield Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 68479-150?
What are the uses for Super Sensitive Shield Spf 30?
Which are Super Sensitive Shield Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Super Sensitive Shield 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DICAPRYLYL ETHER (UNII: 77JZM5516Z)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- OAT (UNII: Z6J799EAJK)
- BOERHAVIA DIFFUSA ROOT (UNII: KR0SR09KYL)
- OXOTHIAZOLIDINE (UNII: M6U1ZG59XD)
- WATERMELON (UNII: 231473QB6R)
- APPLE (UNII: B423VGH5S9)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- LENS CULINARIS FRUIT (UNII: ZYZ076G9JH)
- ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- LAVANDIN OIL (UNII: 9RES347CKG)
- TOCOPHEROL (UNII: R0ZB2556P8)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
- LEVOMENOL (UNII: 24WE03BX2T)
- GINGER (UNII: C5529G5JPQ)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- GLYCERIN (UNII: PDC6A3C0OX)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- 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".