acetaminophen, dextromethorphan hydrobromide, doxylamine succinate and phenylephrine hydrochloride
Generic: acetaminophen, dextromethorphan hydrobromide, doxylamine succinate and phenylephrine hydrochloride
Labeler: softgel healthcare private limitedDrug Facts
Product Profile
Brand Name
acetaminophen, dextromethorphan hydrobromide, doxylamine succinate and phenylephrine hydrochloride
Generic Name
acetaminophen, dextromethorphan hydrobromide, doxylamine succinate and phenylephrine hydrochloride
Labeler
softgel healthcare private limited
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, doxylamine succinate 6.25 mg/1, phenylephrine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
35916-0167
Product ID
35916-0167_47c7e929-e897-88c0-e063-6394a90a5821
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2027-12-31
Marketing Start
2024-08-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
359160167
Hyphenated Format
35916-0167
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
acetaminophen, dextromethorphan hydrobromide, doxylamine succinate and phenylephrine hydrochloride (source: ndc)
Generic Name
acetaminophen, dextromethorphan hydrobromide, doxylamine succinate and phenylephrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 10 mg/1
- 6.25 mg/1
- 5 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (35916-0167-1) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Packages (1)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47c7e929-e897-88c0-e063-6394a90a5821", "openfda": {"upc": ["0335916016716"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "V9BI9B5YI2", "04JA59TNSJ"], "rxcui": ["1297288"], "spl_set_id": ["1fcbafaa-c871-db6d-e063-6394a90aab5e"], "manufacturer_name": ["SOFTGEL HEALTHCARE PRIVATE LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (35916-0167-1) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "35916-0167-1", "marketing_start_date": "20240822"}], "brand_name": "Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate and Phenylephrine Hydrochloride", "product_id": "35916-0167_47c7e929-e897-88c0-e063-6394a90a5821", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "35916-0167", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate and Phenylephrine Hydrochloride", "labeler_name": "SOFTGEL HEALTHCARE PRIVATE LIMITED", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate and Phenylephrine Hydrochloride", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "DOXYLAMINE SUCCINATE", "strength": "6.25 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240822", "listing_expiration_date": "20271231"}