NDC 62864-764 Orajel Toothache Rinse
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62864 - Church & Dwight Canada Corp.
- 62864-764 - Orajel Toothache Rinse
Product Characteristics
Product Packages
NDC Code 62864-764-08
Package Description: 237 mL in 1 BOTTLE
NDC Code 62864-764-16
Package Description: 473.2 mL in 1 BOTTLE
Product Details
What is NDC 62864-764?
What are the uses for Orajel Toothache Rinse?
Which are Orajel Toothache Rinse UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BENZYL ALCOHOL (UNII: LKG8494WBH) (Active Moiety)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Orajel Toothache Rinse 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:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- POLOXAMER 338 (UNII: F75JV2T505)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SORBITOL (UNII: 506T60A25R)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- CALCIUM DISODIUM PYROPHOSPHATE (UNII: T9L63LWS5A)
- MENTHOL (UNII: L7T10EIP3A)
- POTASSIUM SODIUM SACCHARATE (UNII: 73U34YC90U)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
What is the NDC to RxNorm Crosswalk for Orajel Toothache Rinse?
- RxCUI: 1865199 - benzyl alcohol 0.27 % / zinc chloride 0.15 % Mucous Membrane Topical Solution
- RxCUI: 1865199 - benzyl alcohol 2.7 MG/ML / zinc chloride 1.5 MG/ML Mucous Membrane Topical Solution
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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".