Home NDC 52389-153 BackAid
Product NDC 52389-153
11-digit product format 523890153
Labeler code 52389
Product ID 52389-153_32c0bf9d-154f-e502-e063-6294a90a0b35
Type HUMAN OTC DRUG
Nonproprietary name acetaminophen, pamabrom
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Kobayashi Healthcare International, Inc.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 1992-02-01
Substance ACETAMINOPHEN; PAMABROM
Active strength 500; 25 mg/1; mg/1
NDC exclude flag No
Listing certified through 2026-12-31
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 BackAid
Brand name suffix Max
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1 PAMABROM 25 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup UA8U0KJM72 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198449 Internal RxNorm lookup 1356080 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 52389-153-01 BackAidMax 14 in 1 BLISTER PACK TABLET, FILM COATED 14 14 52389-153-03 BackAidMax 38 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 38 14 52389-153-14 BackAidMax 1 in 1 CARTON TABLET, FILM COATED 1 14 52389-153-28 BackAidMax 2 in 1 CARTON TABLET, FILM COATED 2 14 52389-153-35 BackAidMax 5 in 1 CARTON TABLET, FILM COATED 5 14 52389-153-35 BackAidMax 7 in 1 BLISTER PACK TABLET, FILM COATED 7 14 52389-153-38 BackAidMax 1 in 1 CARTON TABLET, FILM COATED 1 14 52389-153-46 BackAidMax 1 in 1 CARTON TABLET, FILM COATED 1 14 52389-153-46 BackAidMax 46 in 1 BOTTLE TABLET, FILM COATED 46 14
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Acetaminophen ACTIVE INGREDIENT 362O9ITL9D BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Pamabrom ACTIVE INGREDIENT UA8U0KJM72 BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Acetaminophen ACTIVE MOIETY 362O9ITL9D BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 BROMOTHEOPHYLLINE ACTIVE MOIETY FZG87K1MQ6 BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Calcium sulfate dihydrate INACTIVE INGREDIENT 4846Q921YM BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Cellulose, microcrystalline INACTIVE INGREDIENT OP1R32D61U BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Croscarmellose sodium INACTIVE INGREDIENT M28OL1HH48 BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 D&C Yellow No. 10 INACTIVE INGREDIENT 35SW5USQ3G BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 FD&C Yellow No. 6 INACTIVE INGREDIENT H77VEI93A8 BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Magnesium oxide INACTIVE INGREDIENT 3A3U0GI71G BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Magnesium silicate INACTIVE INGREDIENT 9B9691B2N9 BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Magnesium stearate INACTIVE INGREDIENT 70097M6I30 BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Mineral oil INACTIVE INGREDIENT T5L8T28FGP BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Polyethylene glycol 600 INACTIVE INGREDIENT NL4J9F21N9 BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Potassium gluconate INACTIVE INGREDIENT 12H3K5QKN9 BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Povidone INACTIVE INGREDIENT FZ989GH94E BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Sodium lauryl sulfate INACTIVE INGREDIENT 368GB5141J BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Sodium starch glycolate type a potato INACTIVE INGREDIENT 5856J3G2A2 BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Sorbitol INACTIVE INGREDIENT 506T60A25R BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Starch, corn INACTIVE INGREDIENT O8232NY3SJ BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Stearic acid INACTIVE INGREDIENT 4ELV7Z65AP BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4 Titanium dioxide INACTIVE INGREDIENT 15FIX9V2JP BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [ALVA-AMCO PHARMACAL COMPANIES, INC.] 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52389-153 BACKAID MAX (ACETAMINOPHEN, PAMABROM) TABLET, FILM COATED [KOBAYASHI HEALTHCARE INTERNATIONAL, INC.] 14 Current NDC, Legacy NDC, 9 package rows 20250416_fb9a5647-b7c9-4820-b148-91060e34cb83.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 23 of 79 · 1,579 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Aspirin 81 mg ASPIRIN HYVEE INC 3e602287-565e-a5b9-e063-6294a90abc17 2026-01-13 Warnings Exact identifier application number: M013 ASPIRIN DELAYED RELEASE 81MG ASPIRIN DELAYED RELEASE 81MG Farmacias De Similares TX LLC 3a8a3efc-f0b3-411c-e063-6394a90a84b7 2026-01-13 Warnings Exact identifier application number: M013 Chewable Aspirin 81 mg ASPIRIN HYVEE INC 459f749f-9d23-8752-e063-6394a90a8c81 2026-01-13 Warnings Exact identifier application number: M013 ASPIRIN 325 mg ASPIRIN HYVEE INC 459d01df-6ff6-cff6-e063-6394a90ab35c 2026-01-13 Warnings Exact identifier application number: M013 Pain Terminator Extra Strength Pain Relief CAFFEINE, ACETAMINOPHEN, ASPIRIN Wildman Business Group 8ffb02d9-92df-4d2f-a367-1c71490807fb 2026-01-12 Warnings Exact identifier application number: M013 Aspirin Packs ASPIRIN Sina Health Inc 2865a2c3-53fc-ab9a-e063-6394a90a1418 2026-01-12 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN PD-Rx Pharmaceuticals, Inc. 64696f65-415e-4ce1-a5b3-70662fbcb002 2026-01-12 Warnings Exact identifier application number: M013 Aspirin enteric coated low dose ASPIRIN Walgreen Company 186a6270-e3de-4499-88a4-5f723fee3e34 2026-01-12 Warnings Exact identifier application number: M013 Tension Headache ACETAMINOPHEN, CAFFEINE Cardinal Health 110, LLC. DBA Leader 96684e3f-a13e-49c3-b437-d2627e528a2d 2026-01-12 Warnings Exact identifier application number: M013 Low Dose Aspirin ASPIRIN Family Dollar Services Inc d35d798e-76f1-454d-86f6-ad11c3bf17d8 2026-01-12 Warnings Exact identifier application number: M013 Xpect Acetaminophen ACETAMINOPHEN Cintas Corporation f4aed854-730e-493d-b523-122156e08dde 2026-01-09 Warnings Exact identifier application number: M013 Aspirin ASPIRIN INVAHEALTH INC e5e8a8d5-9174-7975-e053-2a95a90a9aa6 2026-01-08 Warnings Exact identifier application number: M013 Xpect Cold Relief ACETAMINOPHEN GUAIFENESEIN PHENYLEPHRINE HCL Cintas Corporation 02391d55-32b2-4083-9315-98e9b3650c55 2026-01-08 Warnings Exact identifier application number: M013 pain relief back and body EXTRA STRENGTH ASPIRIN, CAFFEINE Rite Aid Corporation a71392c8-3f5b-4d00-baba-a4055ed68bc1 2026-01-07 Warnings Exact identifier application number: M013 Pain Reliever Extra Strength ACETAMINOPHEN L.N.K. International, Inc. 8fed703a-9de2-4c76-a783-fcf004f9b890 2026-01-07 Warnings Exact identifier application number: M013 Aspirin ASPIRIN Amerisource Bergen c3099892-a8cd-4574-a6f9-041e59e2feae 2026-01-07 Warnings Exact identifier application number: M013 Bactimicina Childrens Pain and Fever ACETAMINOPHEN DLC Laboratories, Inc. bdade270-d813-4178-b594-4951632b6839 2026-01-07 Warnings Exact identifier application number: M013 Goodmeds Extra Strength Pain Relief PM ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE Cabinet Health P.B.C. 02c60967-46d7-49b7-82be-bc3c5fd36484 2026-01-06 Warnings Exact identifier application number: M013 Childrens Acetaminophen ACETAMINOPHEN ARMY AND AIR FORCE EXCHANGE SERVICE a73f8217-9eae-4e2a-b29c-7de3861d0e37 2026-01-06 Warnings Exact identifier application number: M013 Pain Relief Acetaminophen PM ACETAMINOPHEN AND DIPHENHYDRAMINE HCL Rite Aid Corporation f77f0120-4042-4b11-ba9c-cd35e1cd0bee 2026-01-05 Warnings Exact identifier application number: M013
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 52389-153-01 52389015301 14 in 1 BLISTER PACK Historical 52389-153-03 52389015303 38 in 1 BOTTLE, PLASTIC Historical 52389-153-14 52389015314 1 BLISTER PACK in 1 CARTON (52389-153-14) / 14 TABLET, FILM COATED in 1 BLISTER PACK (52389-153-01) 1 blister pack 2011-06-01 0000-00-00 No No Current 52389-153-28 52389015328 2 BLISTER PACK in 1 CARTON (52389-153-28) / 14 TABLET, FILM COATED in 1 BLISTER PACK (52389-153-01) 2 blister pack 2011-03-01 0000-00-00 No No Current 52389-153-35 52389015335 5 BLISTER PACK in 1 CARTON (52389-153-35) / 7 TABLET, FILM COATED in 1 BLISTER PACK 5 blister pack 2011-06-01 0000-00-00 No No Current 52389-153-38 52389015338 1 BOTTLE, PLASTIC in 1 CARTON (52389-153-38) / 38 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52389-153-03) 2010-09-01 0000-00-00 No No Current 52389-153-46 52389015346 1 BOTTLE in 1 CARTON (52389-153-46) / 46 TABLET, FILM COATED in 1 BOTTLE 1 bottle 2016-04-29 0000-00-00 No No Current