Home NDC 62011-0027-1 health mart pain relief
Product NDC 62011-0027
Requested package NDC 62011-0027-1
11-digit product format 620110027
Labeler code 62011
Product ID 62011-0027_c82b84b5-1a16-409a-a474-4718c4be98f0
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Strategic Sourcing Services LLC
Application part343
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2011-11-21
Marketing end 0000-00-00
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2020-12-31
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 Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D HEALTH MART PAIN RELIEF (ACETAMINOPHEN) TABLET, FILM COATED [MCKESSON] 4 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D HEALTH MART PAIN RELIEF (ACETAMINOPHEN) TABLET, FILM COATED [MCKESSON] 4 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 HEALTH MART PAIN RELIEF (ACETAMINOPHEN) TABLET, FILM COATED [MCKESSON] 4 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A HEALTH MART PAIN RELIEF (ACETAMINOPHEN) TABLET, FILM COATED [MCKESSON] 4 POLYVINYL ALCOHOL INACTIVE INGREDIENT 532B59J990 HEALTH MART PAIN RELIEF (ACETAMINOPHEN) TABLET, FILM COATED [MCKESSON] 4 POVIDONES INACTIVE INGREDIENT FZ989GH94E HEALTH MART PAIN RELIEF (ACETAMINOPHEN) TABLET, FILM COATED [MCKESSON] 4 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ HEALTH MART PAIN RELIEF (ACETAMINOPHEN) TABLET, FILM COATED [MCKESSON] 4 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP HEALTH MART PAIN RELIEF (ACETAMINOPHEN) TABLET, FILM COATED [MCKESSON] 4 SUCRALOSE INACTIVE INGREDIENT 96K6UQ3ZD4 HEALTH MART PAIN RELIEF (ACETAMINOPHEN) TABLET, FILM COATED [MCKESSON] 4 TALC INACTIVE INGREDIENT 7SEV7J4R1U HEALTH MART PAIN RELIEF (ACETAMINOPHEN) TABLET, FILM COATED [MCKESSON] 4 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP HEALTH MART PAIN RELIEF (ACETAMINOPHEN) TABLET, FILM COATED [MCKESSON] 4
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 62011-0027-1 62011002701 1 BOTTLE in 1 CARTON (62011-0027-1) > 100 TABLET, FILM COATED in 1 BOTTLE 1 bottle 2011-11-21 0000-00-00 No No Current