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 56 of 79 · 1,579 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Publix Fast Relief Effervescent ASPIRIN, CITRIC ACID, SODIUM BICARBONATE Publix Super Markets Inc. 73051f16-2569-7394-e053-2991aa0a5359 2024-11-13 Warnings Exact identifier application number: M013 Quality Choice Effervescent Antacid and Pain Relief ASPIRIN, CITRIC ACID, SODIUM BICARBONATE Chain Drug Marketing Association 70d265de-ff94-e0e4-e053-2a91aa0a962a 2024-11-13 Warnings Exact identifier application number: M013 Quality Choice Extra Strength Effervescent Antacid and Pain Relief ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE Chain Drug Marketing Association 9f7d0c96-a561-a8a0-e053-2995a90a250b 2024-11-13 Warnings Exact identifier application number: M013 WinCo Foods Effervescent Antacid and Pain Relief ASPIRIN, SODIUM BICARBONATE, CITRIC ACID TABLET WinCo Foods, LLC 0c8a755a-089f-477f-97e9-0dd6fdfbe99d 2024-11-13 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Kroger Company 8fb19444-f0e0-4d26-81e8-6a4b835056d8 2024-11-12 Warnings Exact identifier application number: M013 equate pain reliever ACETAMINOPHEN WALMART INC. 59d01f72-4575-48e2-b914-b6a6456ca7d2 2024-11-11 Warnings Exact identifier application number: M013 pain and fever ACETAMINOPHEN Kroger Company d181560c-1c39-4f2e-8a17-996224ca040f 2024-11-09 Warnings Exact identifier application number: M013 Childrens Tylenol ACETAMINOPHEN Kenvue Brands LLC babcb210-6a47-46ef-b4ea-bdde80411cd3 2024-11-08 Warnings Exact identifier application number: M013 Bayer Genuine Aspirin ASPIRIN Acme United Corporation f7f9dc46-a945-7ae3-e053-6394a90a1192 2024-11-08 Warnings Exact identifier application number: M013 TYLENOL Extra Strength ACETAMINOPHEN Kenvue Brands LLC dd87e342-b0cb-4111-9f15-415dbcda4b77 2024-11-07 Warnings Exact identifier application number: M013 Tylenol Extra Strength ACETAMINOPHEN Kenvue Brands LLC 0c5fdda8-5049-46de-e063-6294a90a592b 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC 46ddbfde-54ab-4373-b832-b9c0620b1e9d 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC 333f6231-3778-4c1f-9558-2afddca22c86 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC 34247a3b-0846-4086-becd-76e630b3b721 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC a51c2deb-c703-4dc8-9255-8ac9fe635170 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC ce0a1fbc-7345-462b-b0da-c7149bdc288c 2024-11-07 Warnings Exact identifier application number: M013 TYLENOL Extra Strength ACETAMINOPHEN Kenvue Brands LLC 015a6179-bacb-452d-b594-4de628ddc11d 2024-11-07 Warnings Exact identifier application number: M013 TYLENOL Regular Strength ACETAMINOPHEN Kenvue Brands LLC de5c6654-56c5-40d3-a286-f04ed47ac7c8 2024-11-07 Warnings Exact identifier application number: M013 Midol Complete ACETAMINOPHEN, CAFFEINE, AND PYRILAMINE MALEATE Acme United Corporation f7bf126d-a6f1-231a-e053-6294a90a04e1 2024-11-07 Warnings Exact identifier application number: M013 CareOne Childrens Acetaminophen ACETAMINOPHEN American Sales Company 49021ae8-9655-4885-9f74-52df4cdcb26f 2024-11-07 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