NDC 61995-2312 Alba Botanica Natural Even Advanced Sea Moss Moisturizer Spf15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61995 - The Hain Celestial Group, Inc.
- 61995-2312 - Alba Botanica Natural Even Advanced Sea Moss Moisturizer Spf15
Product Packages
NDC Code 61995-2312-2
Package Description: 1 TUBE in 1 CARTON / 57 g in 1 TUBE
Product Details
What is NDC 61995-2312?
What are the uses for Alba Botanica Natural Even Advanced Sea Moss Moisturizer Spf15?
Which are Alba Botanica Natural Even Advanced Sea Moss Moisturizer Spf15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Alba Botanica Natural Even Advanced Sea Moss Moisturizer 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CHAMOMILE (UNII: FGL3685T2X)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- HYDROGENATED PALM KERNEL OIL (UNII: FM8D1RE2VP)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- LAMINARIA DIGITATA (UNII: 15E7C67EE8)
- SPIRULINA MAXIMA (UNII: 9K7IG15M0Q)
- MACROCYSTIS PYRIFERA (UNII: K31S3OG5C4)
- ULVA LACTUCA (UNII: PHR3P25W6Y)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ALCOHOL (UNII: 3K9958V90M)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- ALLANTOIN (UNII: 344S277G0Z)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)
- DIACETYL BOLDINE (UNII: 37727Z7M0I)
- ERYTHRITOL (UNII: RA96B954X6)
- HOMARINE HYDROCHLORIDE (UNII: 8866LNG61N)
- MONTMORILLONITE (UNII: A585MN1H2L)
- PANTHENOL (UNII: WV9CM0O67Z)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- BENZYL BENZOATE (UNII: N863NB338G)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
* 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".