Home NDC 50844-413 Back and Body
Product NDC 50844-413
11-digit product format 508440413
Labeler code 50844
Product ID 50844-413_e2623a15-74b3-4895-99a6-eec690b1c531
Type HUMAN OTC DRUG
Nonproprietary name Aspirin, Caffeine
Dosage form TABLET, FILM COATED
Route ORAL
Labeler L.N.K. International, Inc.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2004-04-12
Substance ASPIRIN; CAFFEINE
Active strength 500; 32.5 mg/1; mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]
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 Back and Body
Brand name suffix Extra Strength
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ASPIRIN 500 mg/1 CAFFEINE 32.5 mg/1
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50844-413-08 Back and BodyExtra Strength 1 in 1 CARTON TABLET, FILM COATED 1 13 50844-413-08 Back and BodyExtra Strength 24 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 24 13 50844-413-09 Back and BodyExtra Strength 20 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 20 13 50844-413-09 Back and BodyExtra Strength 1 in 1 CARTON TABLET, FILM COATED 1 13
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ASPIRIN ACTIVE INGREDIENT R16CO5Y76E EXTRA STRENGTH BACK AND BODY (ASPIRIN, CAFFEINE) CAPSULE [L.N.K. INTERNATIONAL, INC.] 1 CAFFEINE ACTIVE INGREDIENT 3G6A5W338E EXTRA STRENGTH BACK AND BODY (ASPIRIN, CAFFEINE) CAPSULE [L.N.K. INTERNATIONAL, INC.] 1 ASPIRIN ACTIVE MOIETY R16CO5Y76E EXTRA STRENGTH BACK AND BODY (ASPIRIN, CAFFEINE) CAPSULE [L.N.K. INTERNATIONAL, INC.] 1 CAFFEINE ACTIVE MOIETY 3G6A5W338E EXTRA STRENGTH BACK AND BODY (ASPIRIN, CAFFEINE) CAPSULE [L.N.K. INTERNATIONAL, INC.] 1 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO EXTRA STRENGTH BACK AND BODY (ASPIRIN, CAFFEINE) CAPSULE [L.N.K. INTERNATIONAL, INC.] 1 MALTODEXTRIN INACTIVE INGREDIENT 7CVR7L4A2D EXTRA STRENGTH BACK AND BODY (ASPIRIN, CAFFEINE) CAPSULE [L.N.K. INTERNATIONAL, INC.] 1 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A EXTRA STRENGTH BACK AND BODY (ASPIRIN, CAFFEINE) CAPSULE [L.N.K. INTERNATIONAL, INC.] 1 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J EXTRA STRENGTH BACK AND BODY (ASPIRIN, CAFFEINE) CAPSULE [L.N.K. INTERNATIONAL, INC.] 1 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ EXTRA STRENGTH BACK AND BODY (ASPIRIN, CAFFEINE) CAPSULE [L.N.K. INTERNATIONAL, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50844-413 BACK AND BODY EXTRA STRENGTH (ASPIRIN, CAFFEINE) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 12 Current NDC, Legacy NDC, 4 package rows 20240921_6d254f3f-8223-4a6e-a3b2-f53f145ff3dc.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 22 of 83 · 1,657 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join basic care aspirin ASPIRIN Amazon.com Services LLC 265c7d85-a666-4234-9c30-ca8e31f4bcb8 2026-02-03 Warnings Exact identifier application number: M013 GOODYS MAX ACETAMINOPHEN, ASPIRIN, AND CAFFEINE Medtech Products Inc. 02b3a604-3f09-47e7-add1-b9038b3a268b 2026-02-02 Warnings Exact identifier application number: M013 Nighttime Pain Reliever plus Sleep Aid ACETAMINOPHEN, DIPHENHYDRAMINE HCL WALMART INC. 8dd85a6b-507c-4502-9e55-a40bdf21d379 2026-02-02 Warnings Exact identifier application number: M013 Pain Reliever ACETAMINOPHEN Rite Aid Corporation 9a647967-f0c6-466e-be70-34fd3de0a803 2026-02-02 Warnings Exact identifier application number: M013 Pain Reliever Extra Strength ACETAMINOPHEN Wal-Mart Stores Inc 72365264-f9c4-49f0-be64-73d95817d358 2026-02-02 Warnings Exact identifier application number: M013 Acetaminophen 325mg ACETAMINOPHEN Marlex Pharmaceuticals Inc 4a18168c-dd36-8280-e063-6394a90a7e10 2026-02-01 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Marlex Pharmaceuticals Inc 4a183b7d-3a1e-5557-e063-6294a90a5493 2026-02-01 Warnings Exact identifier application number: M013 Mejoralito Children CHILDREN ACETAMINOPHEN OPMX LLC 499e2334-fe7b-ed75-e063-6294a90a3e4c 2026-01-30 Warnings Exact identifier application number: M013 Resfriol-ito Children ACETAMINOPHEN OPMX LLC 49a27970-f497-934d-e063-6394a90a08d9 2026-01-30 Warnings Exact identifier application number: M013 DOLODOL ACETAMINOPHEN, ASPIRIN, CAFFEINE OPMX LLC 4c3544bb-058d-4585-e063-6394a90a79f4 2026-01-30 Warnings Exact identifier application number: M013 ATAMEL Forte ACETAMINOPHEN OPMX LLC 4988c97a-af39-16a8-e063-6294a90a8993 2026-01-29 Warnings Exact identifier application number: M013 EXTRA STRENGTH PAIN RELEIF ACETAMINOPHEN Strategic Sourcing Services, LLC 0392db17-c4f3-424b-9dee-549fc5df61c5 2026-01-29 Warnings Exact identifier application number: M013 Regular Strength Pain Reliever ACETAMINOPHEN Strategic Sourcing Services, LLC 959db1b0-2d9f-4857-b475-0fa027365212 2026-01-29 Warnings Exact identifier application number: M013 ASPIRIN ASPIRIN Strategic Sourcing Services LLC 8acdbcf9-64a0-4dda-b60e-7e122254ecf3 2026-01-29 Warnings Exact identifier application number: M013 Crocin MAX ACETAMINOPHEN OPMX LLC 498c7d7e-d952-c122-e063-6394a90ae72f 2026-01-29 Warnings Exact identifier application number: M013 DOLONEURO-TROPAS ACETAMINOPHEN, CAFFEINE OPMX LLC 4c4b0d8c-3195-7d7b-e063-6294a90a8c42 2026-01-29 Warnings Exact identifier application number: M013 Acetaminophen Extra Strength ACETAMINOPHEN FOODHOLD U.S.A., LLC bc19bd47-69ea-4bcc-8d28-c043c9d32513 2026-01-29 Warnings Exact identifier application number: M013 Alka-Seltzer Pain Relief ALKA-SELTZER PAIN RELIEF Bayer HealthCare LLC. 4975f0ff-0480-7fca-e063-6294a90aef2f 2026-01-28 Warnings Exact identifier application number: M013 Extra Strength Mini Softgels Pain Reliever ACETAMINOPHEN THE KROGER CO b49aae4f-b040-44a0-be73-cdf45cf14d7e 2026-01-28 Warnings Exact identifier application number: M013 Extra Strength Acetaminophen ACETAMINOPHEN Preferred Pharmaceuticals Inc. b25faa8c-2d13-450a-970f-81c17a633030 2026-01-28 Warnings Exact identifier application number: M013
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 50844-413-08 50844041308 1 BOTTLE, PLASTIC in 1 CARTON (50844-413-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2004-04-12 0000-00-00 No No Current 50844-413-09 50844041309 1 BOTTLE, PLASTIC in 1 CARTON (50844-413-09) / 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2004-04-12 No No Current