NDC 70112-150 Levigolt
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 70112-150?
What are the uses for Levigolt?
Which are Levigolt UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Levigolt 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:
- ALCOHOL (UNII: 3K9958V90M)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
- CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- GLYCERIN (UNII: PDC6A3C0OX)
- C12-13 PARETH-23 (UNII: J1WW1510L4)
- PROPANEDIOL (UNII: 5965N8W85T)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- C12-13 PARETH-3 (UNII: DMC6N3419L)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
What is the NDC to RxNorm Crosswalk for Levigolt?
- RxCUI: 1595624 - lidocaine HCl 4 % / menthol 1 % Topical Cream
- RxCUI: 1595624 - lidocaine hydrochloride 40 MG/ML / menthol 10 MG/ML Topical Cream
- RxCUI: 1595624 - lidocaine hydrochloride 4 % / menthol 1 % Topical Cream
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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".