NDC 10237-740 Orajel Kids My Way Anticavity Toothpaste
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10237 - Church & Dwight Co., Inc.
- 10237-740 - Orajel
Product Characteristics
Product Packages
NDC Code 10237-740-42
Package Description: 1 TUBE in 1 CARTON / 119 g in 1 TUBE
Product Details
What is NDC 10237-740?
What are the uses for Orajel Kids My Way Anticavity Toothpaste?
Which are Orajel Kids My Way Anticavity Toothpaste UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Orajel Kids My Way Anticavity Toothpaste 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:
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Orajel Kids My Way Anticavity Toothpaste?
- RxCUI: 416783 - sodium fluoride 0.24 % Toothpaste
- RxCUI: 416783 - sodium fluoride 0.0024 MG/MG Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (fluoride ion 0.13 % ) Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (fluoride ion 0.14 % ) Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (fluoride ion 0.15 % ) Toothpaste
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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".