NDC 69942-030 Moroccanoil Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69942 - Moroccanoil, Inc.
- 69942-030 - Moroccanoil Spf 30
Product Packages
NDC Code 69942-030-01
Package Description: 1 BOTTLE in 1 BOX / 150 mL in 1 BOTTLE
Product Details
What is NDC 69942-030?
What are the uses for Moroccanoil Spf 30?
Which are Moroccanoil Spf 30 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)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Moroccanoil Spf 30 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 5 (UNII: 0THT5PCI0R)
- GARDENIA TAITENSIS FLOWER (UNII: T0OCU8201Y)
- GLYCERIN (UNII: PDC6A3C0OX)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COCONUT OIL (UNII: Q9L0O73W7L)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- POLYESTER-7 (UNII: 0841698D2F)
- POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
- HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
- SOYBEAN OIL (UNII: 241ATL177A)
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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".