NDC 57815-031 First Aid Shot Therapy Cold Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57815 - First Aid Beverages, Inc.
- 57815-031 - First Aid Shot Therapy Cold Relief
Product Characteristics
Product Packages
NDC Code 57815-031-01
Package Description: 40 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 57815-031?
What are the uses for First Aid Shot Therapy Cold Relief?
Which are First Aid Shot Therapy Cold Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH)
- DEXTROMETHORPHAN (UNII: 7355X3ROTS) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are First Aid Shot Therapy Cold 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- PECTIN (UNII: 89NA02M4RX)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for First Aid Shot Therapy Cold Relief?
- RxCUI: 1667351 - dextromethorphan HBr 20 MG / menthol 10 MG / phenylephrine HCl 10 MG in 40 mL Oral Solution
- RxCUI: 1667351 - dextromethorphan hydrobromide 0.5 MG/ML / menthol 0.213 MG/ML / phenylephrine hydrochloride 0.25 MG/ML Oral Solution
- RxCUI: 1667351 - dextromethorphan HBr 20 MG / menthol 8.5 MG / phenylephrine HCl 10 MG per 40 ML Oral 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".