NDC 10237-703 Orajel Maximum Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10237 - Church & Dwight Co., Inc.
- 10237-703 - Orajel
Product Packages
NDC Code 10237-703-45
Package Description: 1 BOTTLE, GLASS in 1 CARTON / 13.3 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 10237-703?
What are the uses for Orajel Maximum Strength?
Which are Orajel 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 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:
- ALCOHOL (UNII: 3K9958V90M)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
What is the NDC to RxNorm Crosswalk for Orajel Maximum Strength?
- RxCUI: 1045335 - Orajel For Toothache 20 % Mucous Membrane Topical Solution
- RxCUI: 1045335 - benzocaine 200 MG/ML Mucous Membrane Topical Solution [Orajel]
- RxCUI: 1045335 - Orajel 20 % Mucous Membrane Topical Solution
- RxCUI: 1045335 - Orajel 200 MG/ML Mucous Membrane Topical Solution
- RxCUI: 308657 - benzocaine 20 % 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".