NDC 11822-3788 Icy Hot With Lidocaine No-mess
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11822 - Rite Aid Hdgrts Corp
- 11822-3788 - Icy Hot With Lidocaine No-mess
Product Packages
NDC Code 11822-3788-9
Package Description: 70.8 g in 1 BOTTLE
Product Details
What is NDC 11822-3788?
What are the uses for Icy Hot With Lidocaine No-mess?
Which are Icy Hot With Lidocaine No-mess UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Icy Hot With Lidocaine No-mess 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
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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".