NDC 0363-4004 Walgreens Dark Tanning Oil Sunscreen Spf 4
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0363 - Walgreen Co.
- 0363-4004 - Walgreens Dark Tanning Oil Sunscreen
Product Packages
NDC Code 0363-4004-16
Package Description: 226 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 0363-4004?
What are the uses for Walgreens Dark Tanning Oil Sunscreen Spf 4?
Which are Walgreens Dark Tanning Oil Sunscreen Spf 4 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Walgreens Dark Tanning Oil Sunscreen Spf 4 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:
- MINERAL OIL (UNII: T5L8T28FGP)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- COCONUT OIL (UNII: Q9L0O73W7L)
- AMYL ACETATE (UNII: 92Q24NH7AS)
- PAPAYA (UNII: KU94FIY6JB)
- COLOCASIA ESCULENTA ROOT (UNII: H7B71Q0G0D)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PASSIFLORA INCARNATA FRUIT (UNII: SF206I8G4P)
- GUAVA (UNII: 74O70D6VG0)
- COCOA BUTTER (UNII: 512OYT1CRR)
- MANGO (UNII: I629I3NR86)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- PLUMERIA RUBRA FLOWER (UNII: 8P7XXY759H)
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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".