NDC 69804-080 Extra Strength Numbify Anorectal
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What is NDC 69804-080?
Which are Extra Strength Numbify Anorectal UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Extra Strength Numbify Anorectal 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:
- CARBOMER 940 (UNII: 4Q93RCW27E)
- COCONUT OIL (UNII: Q9L0O73W7L)
- PIPER METHYSTICUM ROOT (UNII: BOW48C81XP)
- CHAMOMILE (UNII: FGL3685T2X)
- BORIC ACID (H3BO3), COMPD. WITH 2,2',2''-NITRILOTRIS(ETHANOL) (1:3) (UNII: 43O5OP619T)
- PINEAPPLE JUICE (UNII: O4KOG0B1KC)
- MARANTA ARUNDINACEA ROOT (UNII: FVN346W31A)
What is the NDC to RxNorm Crosswalk for Extra Strength Numbify Anorectal?
- RxCUI: 1010057 - lidocaine HCl 5 % Topical Gel
- RxCUI: 1010057 - lidocaine hydrochloride 0.05 MG/MG Topical Gel
- RxCUI: 1010057 - lidocaine hydrochloride 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".