NDC 10237-752 Orajel Instant Pain Relief Severe
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What is NDC 10237-752?
What are the uses for Orajel Instant Pain Relief Severe?
Which are Orajel Instant Pain Relief Severe UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Orajel Instant Pain Relief Severe 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:
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GELATIN (UNII: 2G86QN327L)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- MINERAL OIL (UNII: T5L8T28FGP)
- PECTIN (UNII: 89NA02M4RX)
- PETROLATUM (UNII: 4T6H12BN9U)
- POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
What is the NDC to RxNorm Crosswalk for Orajel Instant Pain Relief Severe?
- RxCUI: 1543432 - benzocaine 20 % / menthol 0.5 % / benzalkonium chloride 0.1 % Oral Gel
- RxCUI: 1543432 - benzalkonium chloride 0.001 MG/MG / benzocaine 0.2 MG/MG / menthol 0.005 MG/MG Oral 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".