daytime cold and flu non drowsy

Generic: acetaminophen, dextromethorphan hbr, phenylephrine hcl

Labeler: rite aid corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name daytime cold and flu non drowsy
Generic Name acetaminophen, dextromethorphan hbr, phenylephrine hcl
Labeler rite aid corporation
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, phenylephrine hydrochloride 5 mg/1

Manufacturer
Rite Aid Corporation

Identifiers & Regulatory

Product NDC 11822-3391
Product ID 11822-3391_b185486c-d2e3-4fc4-9d62-ad4eef88e0ba
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2020-04-30
Marketing End 2026-12-30

Pharmacologic Class

Classes
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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 118223391
Hyphenated Format 11822-3391

Supplemental Identifiers

RxCUI
1086997
UPC
0011822339193
UNII
362O9ITL9D 9D2RTI9KYH 04JA59TNSJ

Packaging Origin

Original Packager
true

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 daytime cold and flu non drowsy (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 10 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 24 BLISTER PACK in 1 CARTON (11822-3391-8) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
  • 48 BLISTER PACK in 1 CARTON (11822-3391-9) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (2)

11822-3391-8 24 BLISTER PACK in 1 CARTON (11822-3391-8) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 11822-3391-9 48 BLISTER PACK in 1 CARTON (11822-3391-9) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Ingredients (3)

acetaminophen (325 mg/1) dextromethorphan hydrobromide (10 mg/1) phenylephrine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Daytime Cold and Flu Non Drowsy ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b185486c-d2e3-4fc4-9d62-ad4eef88e0ba", "openfda": {"upc": ["0011822339193"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1086997"], "spl_set_id": ["09bd88ec-ff84-4640-b561-243fda727043"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BLISTER PACK in 1 CARTON (11822-3391-8)  / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "11822-3391-8", "marketing_end_date": "20261230", "marketing_start_date": "20200430"}, {"sample": false, "description": "48 BLISTER PACK in 1 CARTON (11822-3391-9)  / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "11822-3391-9", "marketing_end_date": "20261230", "marketing_start_date": "20200430"}], "brand_name": "Daytime Cold and Flu Non Drowsy", "product_id": "11822-3391_b185486c-d2e3-4fc4-9d62-ad4eef88e0ba", "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": "11822-3391", "generic_name": "Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daytime Cold and Flu", "brand_name_suffix": "Non Drowsy", "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_end_date": "20261230", "marketing_start_date": "20200430"}