up and up mucus relief

Generic: guaifenesin

Labeler: Target Corporation
NDC Directory HUMAN OTC DRUG ANDA Active

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

Identifiers & Regulatory

Product NDC 11673-421
Product ID 11673-421_1d9231c6-12c2-4951-becb-5e2c2da91e79
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA078912
Listing Expiration 2026-12-31
Marketing Start 2020-07-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673421
Hyphenated Format 11673-421

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
  • 1 BOTTLE in 1 CARTON (11673-421-60) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE
source: ndc

Packages (2)

11673-421-01 1 BLISTER PACK in 1 CARTON (11673-421-01) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK 11673-421-60 1 BOTTLE in 1 CARTON (11673-421-60) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE

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": "1d9231c6-12c2-4951-becb-5e2c2da91e79", "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"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-421-60)  / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "11673-421-60", "marketing_start_date": "20200731"}], "brand_name": "up and up mucus relief", "product_id": "11673-421_1d9231c6-12c2-4951-becb-5e2c2da91e79", "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": "20261231"}