backaid

Generic: acetaminophen, caffeine

Labeler: kobayashi healthcare international, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name backaid
Generic Name acetaminophen, caffeine
Labeler kobayashi healthcare international, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1, caffeine 75 mg/1

Manufacturer
Kobayashi Healthcare International, Inc.

Identifiers & Regulatory

Product NDC 52389-253
Product ID 52389-253_41aea851-bb73-0113-e063-6294a90a245f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2024-10-31

Pharmacologic Class

Established (EPC)
central nervous system stimulant [epc] methylxanthine [epc]
Chemical Structure
xanthines [cs]
Physiologic Effect
central nervous system stimulation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52389253
Hyphenated Format 52389-253

Supplemental Identifiers

UPC
0072959530280
UNII
362O9ITL9D 3G6A5W338E
NUI
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 backaid (source: ndc)
Generic Name acetaminophen, caffeine (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 75 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (52389-253-14) / 14 TABLET, FILM COATED in 1 BLISTER PACK
  • 2 BLISTER PACK in 1 CARTON (52389-253-28) / 14 TABLET, FILM COATED in 1 BLISTER PACK
  • 1 BOTTLE, PLASTIC in 1 CARTON (52389-253-38) / 38 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (3)

52389-253-14 1 BLISTER PACK in 1 CARTON (52389-253-14) / 14 TABLET, FILM COATED in 1 BLISTER PACK 52389-253-28 2 BLISTER PACK in 1 CARTON (52389-253-28) / 14 TABLET, FILM COATED in 1 BLISTER PACK 52389-253-38 1 BOTTLE, PLASTIC in 1 CARTON (52389-253-38) / 38 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Ingredients (2)

acetaminophen (500 mg/1) caffeine (75 mg/1)

Linked Drug Pages (1)

BackAid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "41aea851-bb73-0113-e063-6294a90a245f", "openfda": {"nui": ["N0000175739", "N0000175729", "N0000175790", "M0023046"], "upc": ["0072959530280"], "unii": ["362O9ITL9D", "3G6A5W338E"], "spl_set_id": ["25db6bb5-96b6-4be1-e063-6294a90a2300"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_pe": ["Central Nervous System Stimulation [PE]"], "pharm_class_epc": ["Central Nervous System Stimulant [EPC]", "Methylxanthine [EPC]"], "manufacturer_name": ["Kobayashi Healthcare International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (52389-253-14)  / 14 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "52389-253-14", "marketing_start_date": "20241211"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (52389-253-28)  / 14 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "52389-253-28", "marketing_start_date": "20241211"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (52389-253-38)  / 38 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "52389-253-38", "marketing_start_date": "20241211"}], "brand_name": "BackAid", "product_id": "52389-253_41aea851-bb73-0113-e063-6294a90a245f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "52389-253", "generic_name": "acetaminophen, caffeine", "labeler_name": "Kobayashi Healthcare International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BackAid", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "CAFFEINE", "strength": "75 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241031", "listing_expiration_date": "20261231"}