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 | Type |
|---|---|---|---|
| MAX relief junior Grape - ATLANTIC BIOLOGICALS CORP. | ATLANTIC BIOLOGICALS CORP. | 2026-02-13 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17856-1122-1 | MAX relief junior Grape | 50 in 1 BOX, UNIT-DOSE | LIQUID | 50 | 4 | |
| 17856-1122-2 | MAX relief junior Grape | 120 in 1 BOX, UNIT-DOSE | LIQUID | 120 | 4 | |
| 17856-1122-3 | MAX relief junior Grape | 120 in 1 BOX, UNIT-DOSE | LIQUID | 120 | 4 | |
| 17856-1122-4 | MAX relief junior Grape | 72 in 1 BOX, UNIT-DOSE | LIQUID | 72 | 4 | |
| 17856-1122-5 | MAX relief junior Grape | 20.3 mL in 1 CUP, UNIT-DOSE | LIQUID | 20.3 | 4 | |
| 17856-1122-6 | MAX relief junior Grape | 1.25 mL in 1 SYRINGE | LIQUID | 1.25 | 4 | |
| 17856-1122-7 | MAX relief junior Grape | 2.5 mL in 1 SYRINGE | LIQUID | 2.5 | 4 | |
| 17856-1122-8 | MAX relief junior Grape | 15 mL in 1 CUP, UNIT-DOSE | LIQUID | 15 | 4 | |
| 17856-1122-9 | MAX relief junior Grape | 60 in 1 BOX, UNIT-DOSE | LIQUID | 60 | 4 | |
| 17856-1122-9 | MAX relief junior Grape | 1 mL in 1 SYRINGE | LIQUID | 1 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17856-1122 | MAX RELIEF JUNIOR GRAPE (CHILDRENS ACETAMINOPHEN) LIQUID [ATLANTIC BIOLOGICALS CORP.] | 3 | Current NDC, 10 package rows | 20250514_562d7901-44d6-4d9b-be8b-a8d468a22c43.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 17856-1122-1 | ML - Milliliter | 17856-1122 | 6ff0a9b2-03be-4ea1-8611-39fbd5be4f4b | 1 | 2026-02-05 |
| 17856-1122-5 | ML - Milliliter | 17856-1122 | 8df3891c-73a2-47c4-bcee-72eea1317e38 | 1 | 2026-03-17 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| NOTTS - Extra Strength 500 mg | ACETAMINOPHEN | VIVUNT PHARMA LLC | e677f43d-b4ce-e5b0-e053-2a95a90ad67e | 2025-02-12 | Warnings | M013 362O9ITL9D |
| acetaminophen pain reliever fever reducer | ACETAMINOPHEN | Padagis Israel Pharmaceuticals Ltd | b43974c3-4db9-4201-beee-b22596a2b241 | 2025-02-12 | Warnings | 362O9ITL9D |
| DAYTIME COLD AND FLU | DEXTROMETHORPHAN HYDROBROMIDE, ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE | Kroger Company | bc00bbf8-52bb-fa75-e053-2a95a90a9406 | 2025-02-11 | Warnings | 362O9ITL9D |
| Acetaminophen, Aspirin, Caffeine | ACETAMINOPHEN, ASPIRIN, CAFFEINE | LEADER/ Cardinal Health 110, Inc. | b3773f02-02a9-33c8-e053-2995a90a2235 | 2025-02-11 | Warnings | M013 362O9ITL9D |
| Daytime cold and flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCI 325, 10, 5 MG SOFTGELS | TIME CAP LABORATORIES, INC. | fd24653e-c4fa-3c09-e053-6394a90aaa9e | 2025-02-10 | Warnings | 362O9ITL9D |
| EXTRA STRENGTH ACETAMINOPHEN | ACETAMINOPHEN | TIME CAP LABORATORIES, INC. | c9f80d24-bd05-e1ce-e053-2995a90aa646 | 2025-02-10 | Warnings | M013 362O9ITL9D |
| NIGHTTIME COLD AND FLU | DEXTROMETHORPHAN HYDROBROMIDE, ACETAMINOPHEN, DOXYLAMINE SUCCINATE | Kroger Company | bc0115a3-5322-855d-e053-2995a90aba27 | 2025-02-10 | Warnings | 362O9ITL9D |
| Low dose Aspirin | ASPIRIN 81 MG DELAYED RELEASE TABLETS | WALGREENS | c25c55aa-9932-0a55-e053-2a95a90a3d1e | 2025-02-10 | Warnings | M013 |
| AeroTab Pain Reliever | PAIN RELIEVER | Aero Healthcare | 40e2b5ea-a8ea-f1c6-e063-6394a90a1e6f | 2025-02-10 | Warnings | M013 |
| Day time high blood pressure cold and flu | ACETAMINOPHEN DEXTROMETHORPHAN HBR | Camber Consumer Care | 09fbd872-0970-4864-9308-4a7b85983920 | 2025-02-10 | Warnings | 362O9ITL9D |
| Enteric Coated Aspirin Regular Strength | ASPIRIN | Time-Cap Labs, Inc | 5fbd8bb3-46f9-4089-9a21-b6af97a06106 | 2025-02-08 | Warnings | M013 |
| ACETAMINOPHEN | ACETAMINOPHEN | TIME CAP LABS INC | c193dbc0-cc80-4a7c-aa29-457a20edf835 | 2025-02-08 | Warnings | M013 362O9ITL9D |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Honeywell Safety Products, Inc. | 2d90c8e8-f479-3535-e063-6394a90af122 | 2025-02-07 | Warnings | 059QF0KO0R |
| Daytime Severe Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR | Genexa Inc. | 22f23aeb-f874-6e54-e063-6394a90a9565 | 2025-02-07 | Warnings | M013 362O9ITL9D |
| Code Red Eye Drops Redness Relief | POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL | 4 Trees, LLC | 0aa08018-cc2d-d947-e063-6394a90a914a | 2025-02-07 | Warnings | B697894SGQ |
| Tyson 2.0 Mike Red Eye Drops For Dry High Eyes | GLYCERIN, NAPHAZOLINE HCL | Jbrands Pharma L.L.C. | 288e9c85-0562-89bf-e063-6394a90a110d | 2025-02-07 | Warnings | PDC6A3C0OX |
| Pain Relief | ACETAMINOPHEN | BETTER LIVING BRANDS LLC. | f3008928-c555-64ad-e053-2995a90a7307 | 2025-02-05 | Warnings | M013 362O9ITL9D |
| Aspirin 81mg | ASPIRIN | BETTER LIVING BRANDS LLC. | f300dfbc-7137-79d1-e053-2995a90a636e | 2025-02-05 | Warnings | M013 |
| Low dose aspirin 81mg | ASPIRIN | BETTER LIVING BRANDS LLC. | f300c30b-ab1a-a1b4-e053-2a95a90a1294 | 2025-02-05 | Warnings | M013 |
| Hydrocodone Bitartrate and Acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | NuCare Pharmaceuticals,Inc. | fed1eb12-3e39-1bf9-e053-6294a90afd77 | 2025-02-05 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.