NDC 72381-102 Sunscreen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 72381-102?
What are the uses for Sunscreen Spf 30?
Which are Sunscreen Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Sunscreen 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:
- CITRUS AURANTIUM FLOWER (UNII: O730ZX2Z83)
- ORANGE PEEL (UNII: TI9T76XD44)
- LEMON PEEL (UNII: 72O054U628)
- SAGE (UNII: 065C5D077J)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- POTASSIUM STEARATE (UNII: 17V812XK50)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- GLYCERIN (UNII: PDC6A3C0OX)
- CHAMOMILE (UNII: FGL3685T2X)
- THYME (UNII: CW657OBU4N)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CAPRYLYL CAPRYLATE/CAPRATE (UNII: 22MCG4RSMR)
- COCONUT ALKANES (UNII: 1E5KJY107T)
- GLYCERYL DISTEARATE (UNII: 73071MW2KM)
- WATER (UNII: 059QF0KO0R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- LEVOMENOL (UNII: 24WE03BX2T)
What is the NDC to RxNorm Crosswalk for Sunscreen Spf 30?
- RxCUI: 245660 - zinc oxide 15 % Topical Cream
- RxCUI: 245660 - zinc oxide 150 MG/ML Topical Cream
- RxCUI: 245660 - ZNO 150 MG/ML Topical Cream
* 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".