childrens plus multi symptom cold

Generic: acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride

Labeler: walgreens
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name childrens plus multi symptom cold
Generic Name acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride
Labeler walgreens
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

acetaminophen 160 mg/5mL, chlorpheniramine maleate 1 mg/5mL, dextromethorphan hydrobromide 5 mg/5mL, phenylephrine hydrochloride 2.5 mg/5mL

Manufacturer
Walgreens

Identifiers & Regulatory

Product NDC 0363-0034
Product ID 0363-0034_1b2081e6-1591-4f87-a32e-c26e3d90338e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2015-04-30

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc] 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 03630034
Hyphenated Format 0363-0034

Supplemental Identifiers

RxCUI
1113397
UPC
0311917103570
UNII
362O9ITL9D V1Q0O9OJ9Z 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 childrens plus multi symptom cold (source: ndc)
Generic Name acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/5mL
  • 1 mg/5mL
  • 5 mg/5mL
  • 2.5 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (0363-0034-04) / 118 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

0363-0034-04 1 BOTTLE, PLASTIC in 1 BOX (0363-0034-04) / 118 mL in 1 BOTTLE, PLASTIC

Ingredients (4)

acetaminophen (160 mg/5mL) chlorpheniramine maleate (1 mg/5mL) dextromethorphan hydrobromide (5 mg/5mL) phenylephrine hydrochloride (2.5 mg/5mL)

Linked Drug Pages (1)

Childrens Plus Multi Symptom Cold ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b2081e6-1591-4f87-a32e-c26e3d90338e", "openfda": {"upc": ["0311917103570"], "unii": ["362O9ITL9D", "V1Q0O9OJ9Z", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1113397"], "spl_set_id": ["dd967cfb-96b4-4cdc-82e2-a4838001c9e3"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (0363-0034-04)  / 118 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0363-0034-04", "marketing_start_date": "20150430"}], "brand_name": "Childrens Plus Multi Symptom Cold", "product_id": "0363-0034_1b2081e6-1591-4f87-a32e-c26e3d90338e", "dosage_form": "SUSPENSION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "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": "0363-0034", "generic_name": "Acetaminophen, Chlorpheniramine maleate, Dextromethorphan hydrobromide, Phenylephrine hydrochloride", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Childrens Plus Multi Symptom Cold", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}, {"name": "CHLORPHENIRAMINE MALEATE", "strength": "1 mg/5mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "5 mg/5mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "2.5 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150430", "listing_expiration_date": "20261231"}