NDC 66977-107 Regenecare Ha
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66977 - Mpm Medical Llc
- 66977-107 - Regenecare Ha
Product Packages
NDC Code 66977-107-03
Package Description: 85 g in 1 TUBE
Product Details
What is NDC 66977-107?
What are the uses for Regenecare Ha?
Which are Regenecare Ha UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Regenecare Ha 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)
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Regenecare Ha?
- RxCUI: 1011852 - lidocaine HCl 2 % Topical Gel
- RxCUI: 1011852 - lidocaine hydrochloride 0.02 MG/MG Topical Gel
- RxCUI: 1011852 - lidocaine hydrochloride 2 % Topical Jelly
- RxCUI: 2604879 - REGENECARE HA 2 % Topical Gel
- RxCUI: 2604879 - lidocaine hydrochloride 0.02 MG/MG Topical Gel [Regenecare]
* 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".