mucus relief d
Generic: guaifenesin and pseudoephedrine hcl
Labeler: rite aid corporationDrug Facts
Product Profile
Brand Name
mucus relief d
Generic Name
guaifenesin and pseudoephedrine hcl
Labeler
rite aid corporation
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
guaifenesin 1200 mg/1, pseudoephedrine hydrochloride 120 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
11822-7399
Product ID
11822-7399_96276789-815d-44b2-7518-4f1fc101e241
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA208369
Listing Expiration
2026-12-31
Marketing Start
2020-01-15
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
118227399
Hyphenated Format
11822-7399
Supplemental Identifiers
RxCUI
UNII
NUI
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 d (source: ndc)
Generic Name
guaifenesin and pseudoephedrine hcl (source: ndc)
Application Number
ANDA208369 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1200 mg/1
- 120 mg/1
Packaging
- 4 BLISTER PACK in 1 CARTON (11822-7399-4) / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
- 2 BLISTER PACK in 1 CARTON (11822-7399-6) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "96276789-815d-44b2-7518-4f1fc101e241", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ", "6V9V2RYJ8N"], "rxcui": ["1244675"], "spl_set_id": ["82654829-a2a5-06aa-930c-5bdd60e49b10"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Rite Aid Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (11822-7399-4) / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "11822-7399-4", "marketing_start_date": "20200115"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (11822-7399-6) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "11822-7399-6", "marketing_start_date": "20200531"}], "brand_name": "Mucus Relief D", "product_id": "11822-7399_96276789-815d-44b2-7518-4f1fc101e241", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "11822-7399", "generic_name": "Guaifenesin and Pseudoephedrine HCL", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief D", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA208369", "marketing_category": "ANDA", "marketing_start_date": "20200115", "listing_expiration_date": "20261231"}