up and up mucus relief

Generic: guaifenesin

Labeler: target corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name up and up mucus relief
Generic Name guaifenesin
Labeler target corporation
Dosage Form TABLET, MULTILAYER, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

guaifenesin 600 mg/1

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-421
Product ID 11673-421_071469f4-4417-4729-8e75-1536c4dc422f
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA078912
Listing Expiration 2027-12-31
Marketing Start 2020-07-31

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 11673421
Hyphenated Format 11673-421

Supplemental Identifiers

RxCUI
636522
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 up and up mucus relief (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number ANDA078912 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (11673-421-01) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

11673-421-01 1 BLISTER PACK in 1 CARTON (11673-421-01) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (1)

guaifenesin (600 mg/1)

Linked Drug Pages (1)

up and up mucus relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "071469f4-4417-4729-8e75-1536c4dc422f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["7c1598f1-1236-48d2-861b-de4715e3f3d2"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (11673-421-01)  / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "11673-421-01", "marketing_start_date": "20250917"}], "brand_name": "up and up mucus relief", "product_id": "11673-421_071469f4-4417-4729-8e75-1536c4dc422f", "dosage_form": "TABLET, MULTILAYER, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "11673-421", "generic_name": "guaifenesin", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up mucus relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA078912", "marketing_category": "ANDA", "marketing_start_date": "20200731", "listing_expiration_date": "20271231"}