NDC 70692-108 Acetaminophen 500mg, Dextromethorphan Hbr 10mg, Guaifenesin 200mg, Phenylephrine Hcl 5mg
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 70692-108?
What are the uses for Acetaminophen 500mg, Dextromethorphan Hbr 10mg, Guaifenesin 200mg, Phenylephrine Hcl 5mg?
Which are Acetaminophen 500mg, Dextromethorphan Hbr 10mg, Guaifenesin 200mg, Phenylephrine Hcl 5mg UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
- DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH)
- DEXTROMETHORPHAN (UNII: 7355X3ROTS) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
Which are Acetaminophen 500mg, Dextromethorphan Hbr 10mg, Guaifenesin 200mg, Phenylephrine Hcl 5mg 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:
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CROSCARMELLOSE (UNII: 029TFK992N)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- FOOD YELLOW 3 FREE ACID (UNII: G2B7JWK1GG)
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MICA (UNII: V8A1AW0880)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- TALC (UNII: 7SEV7J4R1U)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
What is the NDC to RxNorm Crosswalk for Acetaminophen 500mg, Dextromethorphan Hbr 10mg, Guaifenesin 200mg, Phenylephrine Hcl 5mg?
- RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
- RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
- RxCUI: 1110988 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
* Please review the disclaimer below.
[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".