FDA.reportPublic FDA data

Goodys Back and Body Pain

Product NDC
63029-600
11-digit product format
630290600
Labeler code
63029
Product ID
63029-600_8ec77abf-03a1-4692-959a-0bd779ecdc6c
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen and Asprin
Dosage form
POWDER
Route
ORAL
Labeler
Medtech Products Inc.
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2012-06-01
Substance
ACETAMINOPHEN; ASPIRIN
Active strength
325; 500 mg/1; mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]
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
Goodys Back and Body Pain
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN325 mg/1
ASPIRIN500 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
362O9ITL9DInternal UNII lookup
R16CO5Y76EInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
763111Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
055d0288-61d4-48bc-b91f-6ecc1969beb8Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
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11939cf5-0ea7-5df5-5127-00a7ce07fd7fProduct name520250115
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88300afc-e1c4-ad17-c80b-4957f1b809a5Product name520250113
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
4eddd6ca-259a-4c6c-a3a4-2025015ce043Product name720240611
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
16cde546-8deb-4df2-a072-dab5566ede95Product name120231003
20ab58de-c64a-4ec2-9210-3aa3fae2b66fProduct name120230808
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92ead9ae-674d-4eee-a492-c385d496891fProduct name320220308
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0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
103b151b-b17f-42ac-8624-3ef62f5e2975Product name220200507
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22d922aa-c443-d9f3-b23c-03b03a9ad31cProduct name720181220
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7916de40-e296-41f0-b811-6d0df1a33e2cProduct name920180627
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
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419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
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9425d234-4ae1-4b53-adc6-8cc7af6dd657Product name120150929
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47fd879b-91c5-e1e5-130f-29d082a871ecProduct name120140508
53855190-7124-8179-f018-e792f7c27f28Product name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
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810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
84fb0b3d-1d72-b672-bc70-2b676a23e7e0Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
9007e8a7-ff50-f9b9-7945-f2a1deadd94eProduct name120140508
96c2be53-8e44-452d-56a2-d255b2f1af2dProduct name120140508
96c5169b-5b9d-547d-bf22-d688d91866e4Product name120140508
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c8753a88-edde-8e17-a396-705537b52ceeProduct name120140508
cd4f9ae2-1343-ecd2-ce0f-97db0c2b51ceProduct name120140508
cf3a804d-0326-aa22-0142-c184b5657d85Product name120140508
d83c592c-dd97-4cbf-36ac-13da806684bdProduct name120140508
e01133ad-4dcd-c7f3-454b-2ff569ee160aProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
63029-600-012020-04-08Goodys Back and Body Pain
63029-600-012020-04-08Goodys Back and Body Pain
63029-600-062020-04-08Goodys Back and Body Pain
63029-600-062020-04-08Goodys Back and Body Pain
63029-600-012020-01-31Goodys Back and Body Pain
63029-600-012020-01-31Goodys Back and Body Pain
63029-600-062020-01-31Goodys Back and Body Pain
63029-600-062020-01-31Goodys Back and Body Pain

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63029-600-01Goodys Back and Body Pain24 in 1 BOXPOWDER247
63029-600-06Goodys Back and Body Pain6 in 1 BOXPOWDER67

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63029-600-01EA - Each63029-6006319883d-3183-4ff1-9303-a0c2b2f7937012022-06-06
63029-600-06EA - Each63029-600037bf183-ff1a-44b2-af06-95a2c6e4b57c12022-06-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACETAMINOPHENACTIVE INGREDIENT362O9ITL9DGOODYS BACK AND BODY PAIN (ACETAMINOPHEN AND ASPRIN) POWDER [MEDTECH PRODUCTS INC.]2
ASPIRINACTIVE INGREDIENTR16CO5Y76EGOODYS BACK AND BODY PAIN (ACETAMINOPHEN AND ASPRIN) POWDER [MEDTECH PRODUCTS INC.]2
ACETAMINOPHENACTIVE MOIETY362O9ITL9DGOODYS BACK AND BODY PAIN (ACETAMINOPHEN AND ASPRIN) POWDER [MEDTECH PRODUCTS INC.]2
ASPIRINACTIVE MOIETYR16CO5Y76EGOODYS BACK AND BODY PAIN (ACETAMINOPHEN AND ASPRIN) POWDER [MEDTECH PRODUCTS INC.]2
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XGOODYS BACK AND BODY PAIN (ACETAMINOPHEN AND ASPRIN) POWDER [MEDTECH PRODUCTS INC.]2
POTASSIUM CHLORIDEINACTIVE INGREDIENT660YQ98I10GOODYS BACK AND BODY PAIN (ACETAMINOPHEN AND ASPRIN) POWDER [MEDTECH PRODUCTS INC.]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63029-600GOODYS BACK AND BODY PAIN (ACETAMINOPHEN AND ASPRIN) POWDER [MEDTECH PRODUCTS INC.]6Current NDC, Legacy NDC, 2 package rows20241101_055d0288-61d4-48bc-b91f-6ecc1969beb8.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 53 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pain Relief Extra StrengthACETAMINOPHENDISCOUNT DRUG MARTe6fee238-0b6f-cb84-e053-2995a90a361b2024-12-05WarningsExact identifier
application number: M013
Menstrual Complete Maximum StrengthACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATEL.N.K. International, Inc.379ef03c-3b6a-40c3-b736-99f0537d26c82024-12-05WarningsExact identifier
application number: M013
Pain Reliever Extra StrengthACETAMINOPHENMarc Glassman, Inc.43bf297f-2832-424f-a013-4bfa1d6c03e62024-12-04WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENPrecision Dose, Inc.5a68ab98-720c-479a-a60a-4e594add6c092024-12-04WarningsExact identifier
application number: M013
HEB Effervescent Pain ReliefASPIRINH. E. BUTT GROCERY COMPANY03876c71-60ec-3280-e063-6294a90a62dc2024-12-03WarningsExact identifier
application number: M013
Migrafein FORTEACETAMINOPHEN, CAFFEINEOPMX LLC028875c9-4129-ce2c-e063-6294a90a26cc2024-12-03WarningsExact identifier
application number: M013
Neo-Lubrina FuerteACETAMINOPHEN, CAFFEINEOPMX LLC0288a327-fd4b-1991-e063-6294a90ace502024-12-03WarningsExact identifier
application number: M013
CAFIZETAMOL FORTEACETAMINOPHEN, CAFFEINEOPMX LLC028771d3-a514-f7a5-e063-6394a90ac4f32024-12-03WarningsExact identifier
application number: M013
BuscapinaACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATEOPMX LLC048c4b03-1cf4-b724-e063-6294a90a1cad2024-12-03WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENTopCo Associates LLCecd6df7e-e7e2-446b-85ef-25971281fe312024-12-03WarningsExact identifier
application number: M013
Market Basket Effervescent Pain ReliefASPIRINDEMOULAS SUPER MARKETS, INC.08133bf0-3c8f-e4d0-e063-6294a90af79a2024-12-03WarningsExact identifier
application number: M013
Aspirin Low DoseASPIRINWinCo Foods, LLC4359da13-e851-440b-91b9-6b544bff20d22024-12-03WarningsExact identifier
application number: M013
Low Dose AspirinASPIRINWinCo Foods, LLC5b3e8a78-5357-42ad-811e-b2578b25dc7b2024-12-03WarningsExact identifier
application number: M013
Low Strength Chewable AspirinASPIRINGeri-Care Pharmaceutical Corpcc77b9d1-7874-4ce8-a763-3a0e1c2891de2024-12-03WarningsExact identifier
application number: M013
Good Sense Childrens Pain and FeverACETAMINOPHENL. Perrigo Companyc6b79501-d08b-4430-9545-70da5f5459752024-12-03WarningsExact identifier
application number: M013
AspirinASPIRINChain Drug Marketing Association0e3be5f4-bc1b-4b44-a86a-ace89f6ee5922024-12-02WarningsExact identifier
application number: M013
St. Joseph Chewable Low Dose AspirinASPIRINFoundation Consumer Healthcare LLC248cd302-e380-4837-bdae-9df620b67e8a2024-12-02WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENAAA Pharmaceutical, Inc.2d98e390-4f2a-41cc-b307-3d2f6a3700dd2024-12-02WarningsExact identifier
application number: M013
Acetaminophen PMACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDEAAA Pharmaceutical, Inc.409b5fcd-5880-4dda-85d8-26aeceb4f8ab2024-12-02WarningsExact identifier
application number: M013
AspirinASPIRINAAA Pharmaceutical, Inc.c0c31523-c4c5-43c2-8d72-4d1456c720e92024-12-02WarningsExact identifier
application number: M013

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
763111acetaminophen 325 MG / aspirin 500 MG Oral PowderPSN055d0288-61d4-48bc-b91f-6ecc1969beb87
763111acetaminophen 325 MG / aspirin 500 MG Oral PowderSCD055d0288-61d4-48bc-b91f-6ecc1969beb87
763111APAP 325 MG / ASA 500 MG Oral PowderSY055d0288-61d4-48bc-b91f-6ecc1969beb87
763111APAP 325 MG / aspirin 500 MG Oral PowderSY055d0288-61d4-48bc-b91f-6ecc1969beb87

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63029-600-016302906000124 POWDER in 1 BOX (63029-600-01) 24 powder2012-06-010000-00-00NoNoCurrent
63029-600-06630290600066 POWDER in 1 BOX (63029-600-06) 6 powder2012-06-010000-00-00NoNoCurrent