NDC 73110-106 Sunscreen With Moisturizer Spf-30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 73110-106?
What are the uses for Sunscreen With Moisturizer Spf-30?
Which are Sunscreen With Moisturizer Spf-30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Sunscreen With Moisturizer 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:
- WATER (UNII: 059QF0KO0R)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- XANTHAN GUM (UNII: TTV12P4NEE)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
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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".