NDC 62802-035 Op Dark Tanning Gel 4
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62802 - Sun & Skin Care Research, Llc
- 62802-035 - Op Dark Tanning Gel 4
Product Packages
NDC Code 62802-035-85
Package Description: 251 mL in 1 BOTTLE
Product Details
What is NDC 62802-035?
What are the uses for Op Dark Tanning Gel 4?
Which are Op Dark Tanning Gel 4 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Op Dark Tanning Gel 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:
- CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLPARABEN (UNII: 14255EXE39)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYISOBUTYLENE (2300 MW) (UNII: DSQ2V1DD1K)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
- CARAMEL (UNII: T9D99G2B1R)
- OLIVE OIL (UNII: 6UYK2W1W1E)
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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".