NDC 17630-2013 Hawaiian Tropic Tanning Dry Spf 6
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17630 - Accra-pac, Inc.
- 17630-2013 - Hawaiian Tropic Tanning Dry Spf 6
Product Packages
NDC Code 17630-2013-1
Package Description: 177 mL in 1 CAN
Product Details
What is NDC 17630-2013?
What are the uses for Hawaiian Tropic Tanning Dry Spf 6?
Which are Hawaiian Tropic Tanning Dry Spf 6 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Hawaiian Tropic Tanning Dry Spf 6 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PLUMERIA EXTRACT (UNII: LGC8P2PC4H)
- GUAVA (UNII: 74O70D6VG0)
- PAPAYA (UNII: KU94FIY6JB)
- PASSIFLORA INCARNATA TOP (UNII: CLF5YFS11O)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- CHOCOLATE (UNII: D9108TZ9KG)
- MANGO (UNII: I629I3NR86)
* 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".