capmist dm

Generic: dextromethorphan hydrobromide, guaifenesin and pseudoephedrine hydrochloride

Labeler: capital pharmaceutical, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name capmist dm
Generic Name dextromethorphan hydrobromide, guaifenesin and pseudoephedrine hydrochloride
Labeler capital pharmaceutical, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 15 mg/1, guaifenesin 400 mg/1, pseudoephedrine hydrochloride 60 mg/1

Manufacturer
Capital Pharmaceutical, LLC

Identifiers & Regulatory

Product NDC 29978-601
Product ID 29978-601_45134129-e509-ebf0-e063-6294a90a03cd
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2013-06-20

Pharmacologic Class

Established (EPC)
expectorant [epc]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 29978601
Hyphenated Format 29978-601

Supplemental Identifiers

RxCUI
1426660
UPC
0329978601904
UNII
9D2RTI9KYH 495W7451VQ 6V9V2RYJ8N
NUI
N0000193956 N0000008867 N0000009560

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 capmist dm (source: ndc)
Generic Name dextromethorphan hydrobromide, guaifenesin and pseudoephedrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
  • 400 mg/1
  • 60 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 BOX (29978-601-30) / 15 TABLET in 1 BLISTER PACK
  • 90 TABLET in 1 BOTTLE (29978-601-90)
source: ndc

Packages (2)

29978-601-30 2 BLISTER PACK in 1 BOX (29978-601-30) / 15 TABLET in 1 BLISTER PACK 29978-601-90 90 TABLET in 1 BOTTLE (29978-601-90)

Ingredients (3)

dextromethorphan hydrobromide (15 mg/1) guaifenesin (400 mg/1) pseudoephedrine hydrochloride (60 mg/1)

Linked Drug Pages (1)

Capmist DM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45134129-e509-ebf0-e063-6294a90a03cd", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0329978601904"], "unii": ["9D2RTI9KYH", "495W7451VQ", "6V9V2RYJ8N"], "rxcui": ["1426660"], "spl_set_id": ["63733ac3-859e-4a8e-8717-d852bd303408"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Capital Pharmaceutical, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 BOX (29978-601-30)  / 15 TABLET in 1 BLISTER PACK", "package_ndc": "29978-601-30", "marketing_start_date": "20130620"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (29978-601-90)", "package_ndc": "29978-601-90", "marketing_start_date": "20130620"}], "brand_name": "Capmist DM", "product_id": "29978-601_45134129-e509-ebf0-e063-6294a90a03cd", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "29978-601", "generic_name": "Dextromethorphan Hydrobromide, Guaifenesin and Pseudoephedrine Hydrochloride", "labeler_name": "Capital Pharmaceutical, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Capmist DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "15 mg/1"}, {"name": "GUAIFENESIN", "strength": "400 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130620", "listing_expiration_date": "20261231"}