NDC 17856-1122-01 - MAX relief junior Grape

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
17856-1122
Requested NDC
17856-1122-01
Package NDCs from labels
17856-1122-5, 17856-1122-1, 17856-1122-8, 17856-1122-4, 17856-1122-6, 17856-1122-2, 17856-1122-7, 17856-1122-3, 17856-1122-9, 17856-1122-01
Manufacturer
ATLANTIC BIOLOGICALS CORP.
Effective date
2026-02-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
MAX relief junior Grape - ATLANTIC BIOLOGICALS CORP.ATLANTIC BIOLOGICALS CORP.2026-02-13HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17856-1122-1MAX relief junior Grape50 in 1 BOX, UNIT-DOSELIQUID504
17856-1122-2MAX relief junior Grape120 in 1 BOX, UNIT-DOSELIQUID1204
17856-1122-3MAX relief junior Grape120 in 1 BOX, UNIT-DOSELIQUID1204
17856-1122-4MAX relief junior Grape72 in 1 BOX, UNIT-DOSELIQUID724
17856-1122-5MAX relief junior Grape20.3 mL in 1 CUP, UNIT-DOSELIQUID20.34
17856-1122-6MAX relief junior Grape1.25 mL in 1 SYRINGELIQUID1.254
17856-1122-7MAX relief junior Grape2.5 mL in 1 SYRINGELIQUID2.54
17856-1122-8MAX relief junior Grape15 mL in 1 CUP, UNIT-DOSELIQUID154
17856-1122-9MAX relief junior Grape60 in 1 BOX, UNIT-DOSELIQUID604
17856-1122-9MAX relief junior Grape1 mL in 1 SYRINGELIQUID14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17856-1122MAX RELIEF JUNIOR GRAPE (CHILDRENS ACETAMINOPHEN) LIQUID [ATLANTIC BIOLOGICALS CORP.]3Current NDC, 10 package rows20250514_562d7901-44d6-4d9b-be8b-a8d468a22c43.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
17856-1122-1ML - Milliliter17856-11226ff0a9b2-03be-4ea1-8611-39fbd5be4f4b12026-02-05
17856-1122-5ML - Milliliter17856-11228df3891c-73a2-47c4-bcee-72eea1317e3812026-03-17

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 124 of 207 · 4,128 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Blink Nourish Dry EyeGLYCERINBausch & Lomb Incorporatedcf2b4e19-af0a-472e-9a2d-9b4fa3e9c9a42025-02-25WarningsExact identifier
unii: PDC6A3C0OX
Bufferin Regular Strength Pain ReliefASPIRINGenomma Lab USA3543b2bf-1062-468a-a5dc-eabb2408af8c2025-02-25WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHEN TABLET EXTENDED RELEASEAsclemed USA, Inc.4ef6bc2b-03cf-474f-bb9e-dbb5792ec1972025-02-24WarningsExact identifier
unii: 362O9ITL9D
Calmour Childrens Acetaminophen Strips ChewableACETAMINOPHEN ORAL CHEWABLE 80 MGCalmourae47b027-4f29-45bb-a8bd-8129789328352025-02-22WarningsExact identifier
application number: M013
unii: 362O9ITL9D
HYDROCODONE BITARTRATE AND ACETAMINOPHENHYDROCODONE BITARTRATE AND ACETAMINOPHENDirect Rxdb73b8ed-9747-6a49-e053-2a95a90a93a12025-02-21Adverse reactionsExact identifier
unii: 362O9ITL9D
HYDROCODONE BITARTRATE AND ACETAMINOPHENHYDROCODONE BITARTRATE AND ACETAMINOPHENDirectRxdd934235-3b2a-51ca-e053-2995a90a00162025-02-21Warnings, Adverse reactionsExact identifier
unii: 362O9ITL9D
Infants TYLENOLACETAMINOPHENKenvue Brands LLCf9de7c2f-016b-4f40-8b5e-141ad194be972025-02-20WarningsExact identifier
application number: M013
rxcui: 307668
unii: 362O9ITL9D
Genexa Acetaminophen PM Extra StrengthACETAMINOPHENGenexa Inc.d82cf6f3-a291-ca2b-e053-2a95a90a6de12025-02-20WarningsExact identifier
application number: M013
unii: 362O9ITL9D
Childrens AcetaminophenACETAMINOPHENAdvagen Pharma Limited8b9456c9-a56b-4748-adb8-c66d6bf072e82025-02-19WarningsExact identifier
application number: M013
rxcui: 307668
unii: 362O9ITL9D
ACETAMINOPHEN AND CODEINEACETAMINOPHEN AND CODEINEDirect_Rx8d7d6fa4-cc9f-6b4b-e053-2995a90a72862025-02-19Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 362O9ITL9D
Genexa Childrens AcetaminophenACETAMINOPHENGenexa Inc.d89fd9d8-d88e-3968-e053-2a95a90afc5f2025-02-19WarningsExact identifier
application number: M013
unii: 362O9ITL9D
Acetaminophen and Codeine PhosphateACETAMINOPHEN AND CODEINE PHOSPHATENuCare Pharmaceuticals, Inc.2e88442f-a6a9-a899-e063-6294a90ac08d2025-02-19Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 362O9ITL9D
AcetaminophenACETAMINOPHENPrecision Dose, Inc.debfa787-7a48-48b5-94b0-6128205240322025-02-19WarningsExact identifier
application number: M013
rxcui: 307668
unii: 362O9ITL9D
AcetaminophenACETAMINOPHENPrecision Dose, Inc.b16e5dcf-b290-4ff2-a150-4b875647ec9a2025-02-19WarningsExact identifier
application number: M013
rxcui: 307668
unii: 362O9ITL9D
TYLENOL Extra StrengthACETAMINOPHENKenvue Brands LLCbb6533e5-e6a9-488c-b8ab-a6a06e87ede92025-02-18WarningsExact identifier
application number: M013
unii: 362O9ITL9D
TYLENOL Extra StrengthACETAMINOPHENKenvue Brands LLCc830320e-72ba-48ff-a4cd-250ac5650bf02025-02-18WarningsExact identifier
application number: M013
unii: 362O9ITL9D
Coricidin HBP Cold and FluACETAMINOPHEN AND CHLORPHENIRAMINE MALEATEBayer HealthCare LLC.763a5334-a741-4678-9947-6037766224502025-02-18WarningsExact identifier
unii: 362O9ITL9D
Bestmade Natural Products BM164ACID PHOS, ARUM TRYPH, BALSAMUM PERU, CAUSTICUM, EQUISETUM, GLYCERINUM, HELONIAS DIOBestmade Natural Products2e6e49aa-278e-5499-e063-6394a90a999c2025-02-18WarningsExact identifier
unii: PDC6A3C0OX
Aspirina CapletsASPIRINBayer HealthCare LLC.2e6f5ba8-8e8b-6059-e063-6394a90adcd52025-02-18WarningsExact identifier
application number: M013
Pain Reliever PMACETAMINOPHEN DIPHENHYDRAMINE HCLQUALITY CHOICE (Chain Drug Marketing Association)4897d1df-4fb3-46e2-bbf0-847e964dca0a2025-02-18WarningsExact identifier
unii: 362O9ITL9D

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.