NDC 72934-5071 Dibucaine Hcl 0.5% / Lidocaine 15% / Phenylephrine Hcl 1% / Prilocaine 5%
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What is NDC 72934-5071?
Which are Dibucaine Hcl 0.5% / Lidocaine 15% / Phenylephrine Hcl 1% / Prilocaine 5% UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIBUCAINE HYDROCHLORIDE (UNII: Z97702A5DG)
- DIBUCAINE (UNII: L6JW2TJG99) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- PRILOCAINE (UNII: 046O35D44R)
- PRILOCAINE (UNII: 046O35D44R) (Active Moiety)
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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".