back and body extra strength

Generic: aspirin, caffeine

Labeler: cvs pharmacy
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name back and body extra strength
Generic Name aspirin, caffeine
Labeler cvs pharmacy
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

aspirin 500 mg/1, caffeine 32.5 mg/1

Manufacturer
CVS Pharmacy

Identifiers & Regulatory

Product NDC 59779-143
Product ID 59779-143_1b6a6655-a5f5-4375-91d9-9ba36697cac3
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2004-04-12

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc] platelet aggregation inhibitor [epc] central nervous system stimulant [epc] methylxanthine [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs] xanthines [cs]
Physiologic Effect
decreased prostaglandin production [pe] decreased platelet aggregation [pe] central nervous system stimulation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59779143
Hyphenated Format 59779-143

Supplemental Identifiers

RxCUI
702316
UNII
R16CO5Y76E 3G6A5W338E
NUI
N0000000160 N0000008836 M0001335 N0000175722 N0000175578 N0000008832 N0000175739 N0000175729 N0000175790 M0023046

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name back and body extra strength (source: ndc)
Generic Name aspirin, caffeine (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 32.5 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (59779-143-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

Ingredients (2)

aspirin (500 mg/1) caffeine (32.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b6a6655-a5f5-4375-91d9-9ba36697cac3", "openfda": {"nui": ["N0000000160", "N0000008836", "M0001335", "N0000175722", "N0000175578", "N0000008832", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "unii": ["R16CO5Y76E", "3G6A5W338E"], "rxcui": ["702316"], "spl_set_id": ["749e2be2-594a-4052-8fa5-45c9ade2d23c"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]", "Xanthines [CS]"], "pharm_class_pe": ["Decreased Prostaglandin Production [PE]", "Decreased Platelet Aggregation [PE]", "Central Nervous System Stimulation [PE]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]", "Central Nervous System Stimulant [EPC]", "Methylxanthine [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (59779-143-12)  / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "59779-143-12", "marketing_start_date": "20040412"}], "brand_name": "Back and Body Extra Strength", "product_id": "59779-143_1b6a6655-a5f5-4375-91d9-9ba36697cac3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["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]"], "product_ndc": "59779-143", "generic_name": "Aspirin, Caffeine", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Back and Body", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ASPIRIN", "strength": "500 mg/1"}, {"name": "CAFFEINE", "strength": "32.5 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20040412", "listing_expiration_date": "20261231"}