NDC 61995-2037 Alba Body Daily Shade Spf15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61995 - The Hain Celestial Group, Inc.
- 61995-2037 - Alba Body Daily Shade Spf15
Product Packages
NDC Code 61995-2037-8
Package Description: 340 g in 1 BOTTLE
NDC Code 61995-2037-9
Package Description: 907 g in 1 BOTTLE
Product Details
What is NDC 61995-2037?
What are the uses for Alba Body Daily Shade Spf15?
Which are Alba Body Daily Shade Spf15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Alba Body Daily Shade Spf15 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:
- LACTIC ACID (UNII: 33X04XA5AT)
- ALCOHOL (UNII: 3K9958V90M)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- SHEA BUTTER (UNII: K49155WL9Y)
- ECHINACEA PURPUREA ROOT (UNII: OS64WTR4KU)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ALLANTOIN (UNII: 344S277G0Z)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CHAMOMILE (UNII: FGL3685T2X)
- CUCUMBER (UNII: YY7C30VXJT)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- HYDROGENATED PALM KERNEL OIL (UNII: FM8D1RE2VP)
- SESAME OIL (UNII: QX10HYY4QV)
- JOJOBA OIL (UNII: 724GKU717M)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- PANTHENOL (UNII: WV9CM0O67Z)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
* 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".