NDC 71942-101 Amavara Transparent Mineral Sunscreen Spf30 Earthwell Zinc Technology, Reef Safe
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71942 - Amavara, Inc
- 71942-101 - Amavara Transparent Mineral Sunscreen Spf30
Product Packages
NDC Code 71942-101-01
Package Description: 88.7 mL in 1 BOX
NDC Code 71942-101-03
Package Description: 49 mL in 1 TUBE
Product Details
What is NDC 71942-101?
What are the uses for Amavara Transparent Mineral Sunscreen Spf30 Earthwell Zinc Technology, Reef Safe?
Which are Amavara Transparent Mineral Sunscreen Spf30 Earthwell Zinc Technology, Reef Safe UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Amavara Transparent Mineral Sunscreen Spf30 Earthwell Zinc Technology, Reef Safe 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 CHLORIDE (UNII: 451W47IQ8X)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- GLYCERIN (UNII: PDC6A3C0OX)
- LEVOMENOL (UNII: 24WE03BX2T)
- GINGER (UNII: C5529G5JPQ)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- BENZYLIDENE DIMETHOXYDIMETHYLINDANONE (UNII: 75HIF3C97L)
- CERIC OXIDE (UNII: 619G5K328Y)
- DIMETHICONE 100 (UNII: RO266O364U)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CARAMEL (UNII: T9D99G2B1R)
- 2',3'-DIHYDROXYACETOPHENONE (UNII: 65328I5OQP)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
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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".