NDC 47046-156 Oral Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 47046 - Anicare Pharmaceuticals Pvt. Ltd
- 47046-156 - Oral Pain Relief
Product Packages
NDC Code 47046-156-02
Package Description: 1 TUBE in 1 CARTON / 14 g in 1 TUBE (47046-156-01)
Product Details
What is NDC 47046-156?
What are the uses for Oral Pain Relief?
Which are Oral Pain Relief 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)
Which are Oral Pain Relief 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:
- AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SORBIC ACID (UNII: X045WJ989B)
- WATER (UNII: 059QF0KO0R)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Oral Pain Relief?
- RxCUI: 1595155 - benzocaine 20 % / benzalkonium chloride 0.1 % Oral Gel
- RxCUI: 1595155 - benzalkonium chloride 0.001 MG/MG / benzocaine 0.2 MG/MG Oral Gel
- RxCUI: 1595155 - benzalkonium chloride 0.1 % / benzocaine 20 % Oral Gel
* Please review the disclaimer below.
[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".