mucus relief

Generic: guaifenesin

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

Drug Facts

Product Profile

Brand Name mucus relief
Generic Name guaifenesin
Labeler h e b
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guaifenesin 600 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-935
Product ID 37808-935_884b612b-7aff-4e32-aa00-a77e28346a7f
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207342
Listing Expiration 2026-12-31
Marketing Start 2021-05-28

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 37808935
Hyphenated Format 37808-935

Supplemental Identifiers

RxCUI
636522
UPC
0041220148134
UNII
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 (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number ANDA207342 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (37808-935-40) / 40 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

37808-935-40 1 BOTTLE, PLASTIC in 1 BOX (37808-935-40) / 40 TABLET in 1 BOTTLE, PLASTIC

Ingredients (1)

guaifenesin (600 mg/1)

Linked Drug Pages (1)

Mucus Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "884b612b-7aff-4e32-aa00-a77e28346a7f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0041220148134"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["562b6ab6-4795-4909-8008-e919173844c9"], "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, PLASTIC in 1 BOX (37808-935-40)  / 40 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "37808-935-40", "marketing_start_date": "20210528"}], "brand_name": "Mucus Relief", "product_id": "37808-935_884b612b-7aff-4e32-aa00-a77e28346a7f", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "37808-935", "generic_name": "Guaifenesin", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA207342", "marketing_category": "ANDA", "marketing_start_date": "20210528", "listing_expiration_date": "20261231"}