day time cold and flu relief non drowsy
Generic: acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride
Labeler: safeway, inc.Drug Facts
Product Profile
Brand Name
day time cold and flu relief non drowsy
Generic Name
acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride
Labeler
safeway, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
acetaminophen 325 mg/15mL, dextromethorphan hydrobromide 10 mg/15mL, phenylephrine hydrochloride 5 mg/15mL
Manufacturer
Identifiers & Regulatory
Product NDC
21130-866
Product ID
21130-866_5627f1a1-b04f-4b93-84ff-5494850e1f1d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2015-08-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
21130866
Hyphenated Format
21130-866
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
day time cold and flu relief non drowsy (source: ndc)
Generic Name
acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/15mL
- 10 mg/15mL
- 5 mg/15mL
Packaging
- 237 mL in 1 BOTTLE, PLASTIC (21130-866-08)
- 355 mL in 1 BOTTLE, PLASTIC (21130-866-12)
Packages (2)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5627f1a1-b04f-4b93-84ff-5494850e1f1d", "openfda": {"upc": ["0321130788881"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1113705"], "spl_set_id": ["cc450f89-a156-48e0-82ae-19782f13c2ca"], "manufacturer_name": ["Safeway, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (21130-866-08)", "package_ndc": "21130-866-08", "marketing_start_date": "20150831"}, {"sample": false, "description": "355 mL in 1 BOTTLE, PLASTIC (21130-866-12)", "package_ndc": "21130-866-12", "marketing_start_date": "20150831"}], "brand_name": "Day Time Cold and Flu Relief non drowsy", "product_id": "21130-866_5627f1a1-b04f-4b93-84ff-5494850e1f1d", "dosage_form": "LIQUID", "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": "21130-866", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride", "labeler_name": "Safeway, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Day Time Cold and Flu Relief", "brand_name_suffix": "non drowsy", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/15mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/15mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/15mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150831", "listing_expiration_date": "20261231"}