multi-symptom cold and flu relief daytime

Generic: acetaminophen 325 mg dextromethorphan hbr 10 mg phenylephrine hci 5 mg

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

Drug Facts

Product Profile

Brand Name multi-symptom cold and flu relief daytime
Generic Name acetaminophen 325 mg dextromethorphan hbr 10 mg phenylephrine hci 5 mg
Labeler rite aid
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

Identifiers & Regulatory

Product NDC 11822-1989
Product ID 11822-1989_164a1b51-e8d2-e907-e063-6394a90a6ad1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-09-15

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 118221989
Hyphenated Format 11822-1989

Supplemental Identifiers

RxCUI
1086997
UPC
0011822198806
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 multi-symptom cold and flu relief daytime (source: ndc)
Generic Name acetaminophen 325 mg dextromethorphan hbr 10 mg phenylephrine hci 5 mg (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
  • 2 BLISTER PACK in 1 CARTON (11822-1989-0) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
  • 4 BLISTER PACK in 1 CARTON (11822-1989-9) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (2)

11822-1989-0 2 BLISTER PACK in 1 CARTON (11822-1989-0) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 11822-1989-9 4 BLISTER PACK in 1 CARTON (11822-1989-9) / 12 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)

MULTI-SYMPTOM COLD AND FLU RELIEF DAYTIME ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "164a1b51-e8d2-e907-e063-6394a90a6ad1", "openfda": {"upc": ["0011822198806"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1086997"], "spl_set_id": ["c92dbbbb-d149-1e7e-e053-2a95a90a6f1a"], "manufacturer_name": ["RITE AID"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (11822-1989-0)  / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "11822-1989-0", "marketing_start_date": "20210915"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (11822-1989-9)  / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "11822-1989-9", "marketing_start_date": "20210915"}], "brand_name": "MULTI-SYMPTOM COLD AND FLU RELIEF DAYTIME", "product_id": "11822-1989_164a1b51-e8d2-e907-e063-6394a90a6ad1", "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": "11822-1989", "generic_name": "ACETAMINOPHEN 325 mg DEXTROMETHORPHAN HBr 10 mg PHENYLEPHRINE HCI 5 mg", "labeler_name": "RITE AID", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MULTI-SYMPTOM COLD AND FLU RELIEF 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": "20210915", "listing_expiration_date": "20261231"}