NDC 69303-650 The Organic Pharmacy Cellular Protection Sunscreen Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 69303-650?
Which are The Organic Pharmacy Cellular Protection Sunscreen Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are The Organic Pharmacy Cellular Protection Sunscreen Spf 50 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERIN (UNII: PDC6A3C0OX)
- DOCOSANOL (UNII: 9G1OE216XY)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SHEA BUTTER (UNII: K49155WL9Y)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- OMEGA-3 FATTY ACIDS (UNII: 71M78END5S)
- XANTHAN GUM (UNII: TTV12P4NEE)
- LACTIC ACID (UNII: 33X04XA5AT)
- SOY STEROL (UNII: PL360EPO9J)
- CITRUS MAXIMA SEED (UNII: 083X55C543)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TOCOPHEROL (UNII: R0ZB2556P8)
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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".