NDC 61995-0437 Baby Mineral Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61995 - The Hain Celestial Group, Inc.
- 61995-0437 - Baby Mineral Spf 50
Product Characteristics
Product Packages
NDC Code 61995-0437-4
Package Description: 113 g in 1 TUBE
Product Details
What is NDC 61995-0437?
Which are Baby Mineral Spf 50 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 Baby Mineral Spf 50 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:
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- WATER (UNII: 059QF0KO0R)
- POLYGLYCERYL-2 SESQUIOLEATE (UNII: RHP7Q83BVB)
- C10-18 TRIGLYCERIDES (UNII: 43AGM4PHPI)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- MICA (UNII: V8A1AW0880)
- GLYCERIN (UNII: PDC6A3C0OX)
- LIMONENE, (+/-)- (UNII: 9MC3I34447)
- COCONUT ALKANES (UNII: 1E5KJY107T)
- JUNIPERUS VIRGINIANA OIL (UNII: PAD4FN7P2G)
- O-ANISALDEHYDE (UNII: 7CP821WF2W)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- LEVULINIC ACID (UNII: RYX5QG61EI)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- SHEA BUTTER (UNII: K49155WL9Y)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- SODIUM ANISATE (UNII: F9WFJ28MV9)
- VANILLIN (UNII: CHI530446X)
- ALCOHOL (UNII: 3K9958V90M)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- GERANIOL (UNII: L837108USY)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
- ORANGE OIL (UNII: AKN3KSD11B)
- CHAMOMILE (UNII: FGL3685T2X)
- BENZYL ACETATE (UNII: 0ECG3V79ZJ)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
* 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".