NDC 59735-102 Hangover Good To Go Moisturizer Spf 25
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59735 - Mana Products, Inc.
- 59735-102 - Hangover Good To Go Moisturizer Spf 25
Product Characteristics
Product Packages
NDC Code 59735-102-01
Package Description: 1 TUBE in 1 CARTON / 40 mL in 1 TUBE
Product Details
What is NDC 59735-102?
Which are Hangover Good To Go Moisturizer Spf 25 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
Which are Hangover Good To Go Moisturizer Spf 25 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:
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- CINNAMON BARK OIL (UNII: XE54U569EC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM ACETATE (UNII: 4550K0SC9B)
- LACTOBACILLUS REUTERI (UNII: 9913I24QEE)
- JOJOBA OIL (UNII: 724GKU717M)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SARCOSINE (UNII: Z711V88R5F)
- INULIN (UNII: JOS53KRJ01)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- STEARETH-20 (UNII: L0Q8IK9E08)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PEG-100 STEARATE (UNII: YD01N1999R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- COCONUT WATER (UNII: 267F5Y81NT)
- HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
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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".