NDC 62802-210 No-ad Spf 8 Tanning
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62802 - Sun & Skin Care Research, Llc
- 62802-210 - No-ad Spf 8 Tanning
Product Packages
NDC Code 62802-210-16
Package Description: 475 g in 1 BOTTLE
Product Details
What is NDC 62802-210?
What are the uses for No-ad Spf 8 Tanning?
Which are No-ad Spf 8 Tanning 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 No-ad Spf 8 Tanning 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)
- CANOLA OIL (UNII: 331KBJ17RK)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- COCONUT OIL (UNII: Q9L0O73W7L)
- CARROT SEED OIL (UNII: 595AO13F11)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ETHYLPARABEN (UNII: 14255EXE39)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
* 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".