Mucus Relief

Product NDC
63981-532
Requested package NDC
63981-532-06
11-digit product format
639810532
Labeler code
63981
Product ID
63981-532_c424eb10-165c-449f-b319-4bca639732c8
Type
HUMAN OTC DRUG
Nonproprietary name
Guaifenesin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
COSTCO WHOLESALE CORPORATION
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2005-12-22
Marketing end
0000-00-00
Substance
GUAIFENESIN
Active strength
400 mg/1
Pharmacologic classes
Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage63981-53263981-532-06DDiscontinued by firm2026-10-15

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4fe95224-f543-4dbb-9445-8cca122b48c8Product name120150609
e8718272-64cb-4436-969b-176c3067c8f4Product name120150609
106ff02a-57e1-4c4c-a307-fd582ff4e311Product name120150212

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63981-532-06EA - Each63981-532fd4f4b76-3260-4540-acfb-b73dc9a8706612012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
GUAIFENESINACTIVE INGREDIENT495W7451VQMUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION]4
GUAIFENESINACTIVE MOIETY495W7451VQMUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION]4
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UMUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION]4
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBDMUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION]4
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOMUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION]4
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION]4
MALTODEXTRININACTIVE INGREDIENT7CVR7L4A2DMUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION]4
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1AMUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION]4
POVIDONESINACTIVE INGREDIENTFZ989GH94EMUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION]4
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION]4
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION]4
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APMUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION]4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63981-532MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION]15Legacy NDC20241109_7b543988-7f16-433a-9eaf-a09d3ecaed05.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
63981-532-06639810532062 BOTTLE, PLASTIC in 1 CARTON (63981-532-06) > 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC2005-12-220000-00-00NoNoCurrent