mucus relief maximum strength

Generic: guaifenesin

Labeler: care one (american sales company)
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief maximum strength
Generic Name guaifenesin
Labeler care one (american sales company)
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guaifenesin 1200 mg/1

Manufacturer
Care One (American Sales Company)

Identifiers & Regulatory

Product NDC 41520-732
Product ID 41520-732_72cc5e09-dd68-4158-935a-4fa739235045
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207342
Listing Expiration 2026-12-31
Marketing Start 2018-12-31

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 41520732
Hyphenated Format 41520-732

Supplemental Identifiers

RxCUI
310621
UPC
0341520004810
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 guaifenesin (source: ndc)
Application Number ANDA207342 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1200 mg/1
source: ndc
Packaging
  • 14 BLISTER PACK in 1 CARTON (41520-732-14) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

41520-732-14 14 BLISTER PACK in 1 CARTON (41520-732-14) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

guaifenesin (1200 mg/1)

Linked Drug Pages (1)

Mucus Relief Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "72cc5e09-dd68-4158-935a-4fa739235045", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0341520004810"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["c94e3943-20da-4bd4-b0ff-6aa60b03a1bf"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Care One (American Sales Company)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 BLISTER PACK in 1 CARTON (41520-732-14)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "41520-732-14", "marketing_start_date": "20181231"}], "brand_name": "Mucus Relief Maximum Strength", "product_id": "41520-732_72cc5e09-dd68-4158-935a-4fa739235045", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "41520-732", "generic_name": "Guaifenesin", "labeler_name": "Care One (American Sales Company)", "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": "ANDA207342", "marketing_category": "ANDA", "marketing_start_date": "20181231", "listing_expiration_date": "20261231"}