mucus relief dm

Generic: guaifenesin, dextromethorphan hbr

Labeler: h e b
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief dm
Generic Name guaifenesin, dextromethorphan hbr
Labeler h e b
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 30 mg/1, guaifenesin 600 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-733
Product ID 37808-733_d2aca5b5-2bb6-41b5-a614-f470d233c98e
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA209692
Listing Expiration 2026-12-31
Marketing Start 2023-02-28

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 37808733
Hyphenated Format 37808-733

Supplemental Identifiers

RxCUI
1298324
UPC
0041220753178
UNII
9D2RTI9KYH 495W7451VQ
NUI
N0000193956 N0000008867 N0000009560

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, dextromethorphan hbr (source: ndc)
Application Number ANDA209692 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
  • 600 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (37808-733-20) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 BOX (37808-733-40) / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

37808-733-20 1 BOTTLE, PLASTIC in 1 BOX (37808-733-20) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC 37808-733-40 1 BOTTLE, PLASTIC in 1 BOX (37808-733-40) / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

Ingredients (2)

dextromethorphan hydrobromide (30 mg/1) guaifenesin (600 mg/1)

Linked Drug Pages (1)

Mucus Relief DM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d2aca5b5-2bb6-41b5-a614-f470d233c98e", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0041220753178"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["bcc41783-9213-4a8e-b7db-75b4da08551d"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["H E B"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-733-20)  / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "37808-733-20", "marketing_start_date": "20230228"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-733-40)  / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "37808-733-40", "marketing_start_date": "20230228"}], "brand_name": "Mucus Relief DM", "product_id": "37808-733_d2aca5b5-2bb6-41b5-a614-f470d233c98e", "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": "37808-733", "generic_name": "Guaifenesin, Dextromethorphan HBr", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}, {"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA209692", "marketing_category": "ANDA", "marketing_start_date": "20230228", "listing_expiration_date": "20261231"}