Home NDC 63981-532-03 Mucus Relief
Product NDC 63981-532
Requested package NDC 63981-532-03
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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded GUAIFENESIN ACTIVE INGREDIENT 495W7451VQ MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION] 4 GUAIFENESIN ACTIVE MOIETY 495W7451VQ MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION] 4 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION] 4 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION] 4 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION] 4 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION] 4 MALTODEXTRIN INACTIVE INGREDIENT 7CVR7L4A2D MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION] 4 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION] 4 POVIDONES INACTIVE INGREDIENT FZ989GH94E MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION] 4 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION] 4 SODIUM STARCH GLYCOLATE TYPE A POTATO INACTIVE INGREDIENT 5856J3G2A2 MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION] 4 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION] 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63981-532 MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [COSTCO WHOLESALE CORPORATION] 15 Legacy NDC 20241109_7b543988-7f16-433a-9eaf-a09d3ecaed05.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63981-532-03 63981053203 1 BLISTER PACK in 1 CARTON (63981-532-03) > 10 TABLET, FILM COATED in 1 BLISTER PACK 1 blister pack 2005-12-22 0000-00-00 Yes No Current