NDC 10237-705 Orajel For Toothache Maximum Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10237 - Church & Dwight Co., Inc.
- 10237-705 - Orajel For Toothache
Product Packages
NDC Code 10237-705-12
Package Description: 12 APPLICATOR in 1 CARTON / 1.8 mL in 1 APPLICATOR
Product Details
What is NDC 10237-705?
What are the uses for Orajel For Toothache Maximum Strength?
Which are Orajel For Toothache Maximum Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Orajel For Toothache Maximum Strength 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:
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- WATER (UNII: 059QF0KO0R)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Orajel For Toothache Maximum Strength?
- RxCUI: 798072 - benzocaine 20 % Medicated Pad
- RxCUI: 798072 - benzocaine 200 MG/ML Medicated Pad
- RxCUI: 798072 - benzocaine 20 % Mucous Membrane Medicated Swab
- RxCUI: 798169 - Orajel 20 % Medicated Pad
- RxCUI: 798169 - benzocaine 200 MG/ML Medicated Pad [Orajel]
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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".