mucus relief dm

Generic: guaifenesin and dextromethorphan hbr

Labeler: ahold u.s.a., inc,
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief dm
Generic Name guaifenesin and dextromethorphan hbr
Labeler ahold u.s.a., inc,
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 60 mg/1, guaifenesin 1200 mg/1

Manufacturer
Ahold U.S.A., Inc,

Identifiers & Regulatory

Product NDC 60000-057
Product ID 60000-057_9c159223-d3f0-48ae-9e4f-f5896838c034
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA206941
Listing Expiration 2026-12-31
Marketing Start 2017-03-17

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 60000057
Hyphenated Format 60000-057

Supplemental Identifiers

RxCUI
1099074
UNII
9D2RTI9KYH 495W7451VQ
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 mucus relief dm (source: ndc)
Generic Name guaifenesin and dextromethorphan hbr (source: ndc)
Application Number ANDA206941 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
  • 1200 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (60000-057-65) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (2)

dextromethorphan hydrobromide (60 mg/1) guaifenesin (1200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9c159223-d3f0-48ae-9e4f-f5896838c034", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["738bbea4-4243-4cbd-980e-a22451b85c4c"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Ahold U.S.A., Inc,"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (60000-057-65)  / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "60000-057-65", "marketing_start_date": "20170317"}], "brand_name": "Mucus Relief DM", "product_id": "60000-057_9c159223-d3f0-48ae-9e4f-f5896838c034", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["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]"], "product_ndc": "60000-057", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "Ahold U.S.A., Inc,", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA206941", "marketing_category": "ANDA", "marketing_start_date": "20170317", "listing_expiration_date": "20261231"}