Home NDC 37808-195 Pain Relief
Product NDC 37808-195
11-digit product format 378080195
Labeler code 37808
Product ID 37808-195_eef88a02-d62d-47e1-85f1-16d3d20e86d1
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, COATED
Route ORAL
Labeler H E B
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2004-05-10
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Pain Relief
Brand name suffix Extra Strength
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198440 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 37808-195-08 Pain ReliefExtra Strength 24 in 1 BOTTLE, PLASTIC TABLET, COATED 24 18 37808-195-08 Pain ReliefExtra Strength 1 in 1 CARTON TABLET, COATED 1 18 37808-195-12 Pain ReliefExtra Strength 1 in 1 CARTON TABLET, COATED 1 18 37808-195-12 Pain ReliefExtra Strength 100 in 1 BOTTLE, PLASTIC TABLET, COATED 100 18 37808-195-20 Pain ReliefExtra Strength 225 in 1 BOTTLE, PLASTIC TABLET, COATED 225 18
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-195 PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET, COATED [H E B] 17 Current NDC, Legacy NDC, 5 package rows 20250406_99699cd6-ba7d-4db0-9f0f-0f2c1a369138.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 83 · 1,657 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 37808-195-08 37808019508 1 BOTTLE, PLASTIC in 1 CARTON (37808-195-08) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC 2004-05-10 0000-00-00 No No Current 37808-195-12 37808019512 1 BOTTLE, PLASTIC in 1 CARTON (37808-195-12) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 2004-05-10 0000-00-00 No No Current 37808-195-20 37808019520 225 TABLET, COATED in 1 BOTTLE, PLASTIC (37808-195-20) 2004-05-10 0000-00-00 No No Current