NDC 62802-172 Ocean Potion Instant Burn Relief Ice
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62802 - Sun & Skin Care Research, Llc
- 62802-172 - Ocean Potion Instant Burn Relief Ice
Product Packages
NDC Code 62802-172-65
Package Description: 605 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 62802-172?
What are the uses for Ocean Potion Instant Burn Relief Ice?
Which are Ocean Potion Instant Burn Relief Ice UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Ocean Potion Instant Burn Relief Ice 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:
- WATER (UNII: 059QF0KO0R)
- ISOCETETH-20 (UNII: O020065R7Z)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- MENTHOL (UNII: L7T10EIP3A)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TROLAMINE (UNII: 9O3K93S3TK)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- COMFREY LEAF (UNII: DG4F8T839X)
- TEA TREE OIL (UNII: VIF565UC2G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Ocean Potion Instant Burn Relief Ice?
- RxCUI: 1011849 - lidocaine HCl 0.5 % Topical Gel
- RxCUI: 1011849 - lidocaine hydrochloride 0.005 MG/MG Topical Gel
- RxCUI: 1011849 - lidocaine hydrochloride 0.5 % Topical Gel
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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".