NDC 71160-011 Spf 30 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71160 - Tekweld Solutions, Inc.
- 71160-011 - Spf 30 Sunscreen
Product Packages
NDC Code 71160-011-00
Package Description: 10 mL in 1 BOTTLE
Product Details
What is NDC 71160-011?
What are the uses for Spf 30 Sunscreen?
Which are Spf 30 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Spf 30 Sunscreen 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)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- ISOCETYL PALMITATE (UNII: 355356620Z)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
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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".