mucus relief dm

Generic: dextromethorphan hbr, guaifenesin

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

Drug Facts

Product Profile

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

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

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-812
Product ID 37808-812_da8f4a08-6e64-44f6-8830-705e3fbdc05e
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207602
Listing Expiration 2026-12-31
Marketing Start 2018-06-25

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 37808812
Hyphenated Format 37808-812

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 dextromethorphan hbr, guaifenesin (source: ndc)
Application Number ANDA207602 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
  • 1200 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (37808-812-66) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
source: ndc

Packages (1)

37808-812-66 1 BOTTLE in 1 CARTON (37808-812-66) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE

Ingredients (2)

dextromethorphan hydrobromide (60 mg/1) guaifenesin (1200 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": "da8f4a08-6e64-44f6-8830-705e3fbdc05e", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["da8f4a08-6e64-44f6-8830-705e3fbdc05e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-812-66)  / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "37808-812-66", "marketing_start_date": "20180625"}], "brand_name": "mucus relief dm", "product_id": "37808-812_da8f4a08-6e64-44f6-8830-705e3fbdc05e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "37808-812", "generic_name": "dextromethorphan HBr, guaifenesin", "labeler_name": "H E B", "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": "ANDA207602", "marketing_category": "ANDA", "marketing_start_date": "20180625", "listing_expiration_date": "20261231"}