NDC 69804-021 Extra Strength Numbing Gel
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 69804-021?
Which are Extra Strength Numbing Gel 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 Numbing Gel 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:
- WITCH HAZEL (UNII: 101I4J0U34)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- AMORPHOPHALLUS KONJAC ROOT (UNII: F7KU2UY3HE)
- CALCIUM HYDROXIDE (UNII: PF5DZW74VN)
- ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
What is the NDC to RxNorm Crosswalk for Extra Strength Numbing Gel?
- RxCUI: 1010077 - lidocaine HCl 4 % Topical Gel
- RxCUI: 1010077 - lidocaine hydrochloride 0.04 MG/MG Topical Gel
- RxCUI: 1010077 - lidocaine hydrochloride 4 % 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".