cold and flu relief daytime
Generic: acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride
Labeler: h e bDrug Facts
Product Profile
Brand Name
cold and flu relief daytime
Generic Name
acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride
Labeler
h e b
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, phenylephrine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
37808-864
Product ID
37808-864_7d85236a-5031-43f2-a4d3-1218fe95a198
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2016-05-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808864
Hyphenated Format
37808-864
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
cold and flu relief daytime (source: ndc)
Generic Name
acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 10 mg/1
- 5 mg/1
Packaging
- 16 BLISTER PACK in 1 CARTON (37808-864-16) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7d85236a-5031-43f2-a4d3-1218fe95a198", "openfda": {"upc": ["0041220385935"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1086997"], "spl_set_id": ["12ace982-bd47-49b0-ba1b-e0a29d42f1d6"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "16 BLISTER PACK in 1 CARTON (37808-864-16) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "37808-864-16", "marketing_start_date": "20160531"}], "brand_name": "Cold and Flu Relief Daytime", "product_id": "37808-864_7d85236a-5031-43f2-a4d3-1218fe95a198", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Adrenergic alpha1-Agonists [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": "37808-864", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cold and Flu Relief", "brand_name_suffix": "Daytime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160531", "listing_expiration_date": "20261231"}