NDC 51147-5010 Becca Mineral Spf Primer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51147 - Becca, Inc.
- 51147-5010 - Becca
Product Packages
NDC Code 51147-5010-2
Package Description: 1 BOTTLE in 1 BOX / 50 mL in 1 BOTTLE (51147-5010-1)
Product Details
What is NDC 51147-5010?
What are the uses for Becca Mineral Spf Primer?
Which are Becca Mineral Spf Primer 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 Becca Mineral Spf Primer 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:
- CYCLOMETHICONE (UNII: NMQ347994Z)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERYL DISTEARATE (UNII: 73071MW2KM)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- UBIDECARENONE (UNII: EJ27X76M46)
- WATER (UNII: 059QF0KO0R)
* 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".