advil allergy and congestion relief

Generic: chlorpheniramine maleate, ibuprofen, phenylephrine hydrochloride

Labeler: navajo manufacturing company inc.
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name advil allergy and congestion relief
Generic Name chlorpheniramine maleate, ibuprofen, phenylephrine hydrochloride
Labeler navajo manufacturing company inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

chlorpheniramine maleate 4 mg/1, ibuprofen 200 mg/1, phenylephrine hydrochloride 10 mg/1

Manufacturer
Navajo Manufacturing Company Inc.

Identifiers & Regulatory

Product NDC 67751-149
Product ID 67751-149_f6f71bb0-5bac-59f7-e053-6394a90abf8e
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA022113
Listing Expiration 2026-12-31
Marketing Start 2016-09-16

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67751149
Hyphenated Format 67751-149

Supplemental Identifiers

RxCUI
1310503
UNII
V1Q0O9OJ9Z WK2XYI10QM 04JA59TNSJ
NUI
N0000000160 M0001335 N0000175722

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 advil allergy and congestion relief (source: ndc)
Generic Name chlorpheniramine maleate, ibuprofen, phenylephrine hydrochloride (source: ndc)
Application Number NDA022113 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
  • 200 mg/1
  • 10 mg/1
source: ndc
Packaging
  • 1 POUCH in 1 CARTON (67751-149-01) / 1 TABLET, COATED in 1 POUCH
  • 2 POUCH in 1 CARTON (67751-149-02) / 1 TABLET, COATED in 1 POUCH
source: ndc

Packages (2)

67751-149-01 1 POUCH in 1 CARTON (67751-149-01) / 1 TABLET, COATED in 1 POUCH 67751-149-02 2 POUCH in 1 CARTON (67751-149-02) / 1 TABLET, COATED in 1 POUCH

Ingredients (3)

chlorpheniramine maleate (4 mg/1) ibuprofen (200 mg/1) phenylephrine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Advil Allergy and Congestion Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f6f71bb0-5bac-59f7-e053-6394a90abf8e", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["V1Q0O9OJ9Z", "WK2XYI10QM", "04JA59TNSJ"], "rxcui": ["1310503"], "spl_set_id": ["d40bf078-ee6f-4c64-9c74-e4e770c150bf"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Navajo Manufacturing Company Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (67751-149-01)  / 1 TABLET, COATED in 1 POUCH", "package_ndc": "67751-149-01", "marketing_start_date": "20160916"}, {"sample": false, "description": "2 POUCH in 1 CARTON (67751-149-02)  / 1 TABLET, COATED in 1 POUCH", "package_ndc": "67751-149-02", "marketing_start_date": "20160916"}], "brand_name": "Advil Allergy and Congestion Relief", "product_id": "67751-149_f6f71bb0-5bac-59f7-e053-6394a90abf8e", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "67751-149", "generic_name": "CHLORPHENIRAMINE MALEATE, IBUPROFEN, PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Navajo Manufacturing Company Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Advil Allergy and Congestion Relief", "active_ingredients": [{"name": "CHLORPHENIRAMINE MALEATE", "strength": "4 mg/1"}, {"name": "IBUPROFEN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA022113", "marketing_category": "NDA", "marketing_start_date": "20160916", "listing_expiration_date": "20261231"}