NDC 76168-100 Hot And Cold With Lidocaine Pain Relieving
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76168 - Velocity Pharma Llc
- 76168-100 - Hot And Cold With Lidocaine
Product Packages
NDC Code 76168-100-30
Package Description: 1 TUBE in 1 CARTON / 76.5 g in 1 TUBE
NDC Code 76168-100-33
Package Description: 1 TUBE in 1 CARTON / 28.35 g in 1 TUBE
Product Details
What is NDC 76168-100?
What are the uses for Hot And Cold With Lidocaine Pain Relieving?
Which are Hot And Cold With Lidocaine Pain Relieving 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 Hot And Cold With Lidocaine Pain Relieving 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:
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETETH-2 (UNII: 7H8VAM7778)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBIC ACID (UNII: X045WJ989B)
- PETROLATUM (UNII: 4T6H12BN9U)
What is the NDC to RxNorm Crosswalk for Hot And Cold With Lidocaine Pain Relieving?
- 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".