mucus relief maximum strength

Generic: mucus relief

Labeler: allegiant health
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief maximum strength
Generic Name mucus relief
Labeler allegiant health
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

guaifenesin 1200 mg/1

Manufacturer
Allegiant Health

Identifiers & Regulatory

Product NDC 69168-460
Product ID 69168-460_da2863ab-6f89-4220-aa26-9fcd69f7cc5b
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA213420
Listing Expiration 2026-12-31
Marketing Start 2024-04-23

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 69168460
Hyphenated Format 69168-460

Supplemental Identifiers

RxCUI
310621
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 maximum strength (source: ndc)
Generic Name mucus relief (source: ndc)
Application Number ANDA213420 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1200 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69168-460-32)
  • 50 TABLET, EXTENDED RELEASE in 1 BOTTLE (69168-460-50)
  • 200 TABLET, EXTENDED RELEASE in 1 BOTTLE (69168-460-98)
source: ndc

Packages (3)

Ingredients (1)

guaifenesin (1200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "da2863ab-6f89-4220-aa26-9fcd69f7cc5b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["3d6c30d7-cd02-44a2-b48e-cd65f2896bfd"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Allegiant Health"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69168-460-32)", "package_ndc": "69168-460-32", "marketing_start_date": "20240423"}, {"sample": false, "description": "50 TABLET, EXTENDED RELEASE in 1 BOTTLE (69168-460-50)", "package_ndc": "69168-460-50", "marketing_start_date": "20240423"}, {"sample": false, "description": "200 TABLET, EXTENDED RELEASE in 1 BOTTLE (69168-460-98)", "package_ndc": "69168-460-98", "marketing_start_date": "20250307"}], "brand_name": "Mucus Relief Maximum Strength", "product_id": "69168-460_da2863ab-6f89-4220-aa26-9fcd69f7cc5b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "69168-460", "generic_name": "Mucus Relief", "labeler_name": "Allegiant Health", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA213420", "marketing_category": "ANDA", "marketing_start_date": "20240423", "listing_expiration_date": "20261231"}