NDC 71521-393 Diabetic First Aid Gel Professional
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 71521-393?
What are the uses for Diabetic First Aid Gel Professional?
Which are Diabetic First Aid Gel Professional UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Diabetic First Aid Gel Professional 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:
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ALCOHOL (UNII: 3K9958V90M)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- GLYCERIN (UNII: PDC6A3C0OX)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- DITTRICHIA VISCOSA WHOLE (UNII: 3SYW69FH88)
What is the NDC to RxNorm Crosswalk for Diabetic First Aid Gel Professional?
- RxCUI: 2535510 - benzalkonium chloride 0.13 % / lidocaine hydrochloride 0.5 % Topical Gel
- RxCUI: 2535510 - benzalkonium chloride 0.0013 MG/MG / lidocaine hydrochloride 0.005 MG/MG 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".