NDC 51672-2131-01 - Childrens Loratadine Sugar Free
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
- 51672-2131
- Requested NDC
- 51672-2131-01
- Package NDCs from labels
- 51672-2131-4, 51672-2131-8, 51672-2131-1, 51672-2131-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | Taro Pharmaceutical Industries, Ltd.
- Effective date
- 2026-08-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Childrens Loratadine Oral Solution Sugar Free | Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | Taro Pharmaceutical Industries, Ltd. | 2026-08-30 | HUMAN OTC DRUG LABEL |
| Childrens Loratadine Oral Solution Sugar Free | Preferred Pharmaceuticals Inc. | 2026-01-15 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-2131-1 | Childrens LoratadineSugar Free | 1 in 1 CARTON | SOLUTION | 1 | 4 | |
| 51672-2131-1 | Childrens LoratadineSugar Free | 240 mL in 1 BOTTLE | SOLUTION | 240 | 4 | |
| 51672-2131-4 | Childrens LoratadineSugar Free | 60 mL in 1 BOTTLE | SOLUTION | 60 | 4 | |
| 51672-2131-4 | Childrens LoratadineSugar Free | 1 in 1 CARTON | SOLUTION | 1 | 4 | |
| 51672-2131-8 | Childrens LoratadineSugar Free | 120 mL in 1 BOTTLE | SOLUTION | 120 | 4 | |
| 51672-2131-8 | Childrens LoratadineSugar Free | 1 in 1 CARTON | SOLUTION | 1 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-2131 | CHILDRENS LORATADINE SUGAR FREE (LORATADINE) SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.] | 3 | Current NDC, Legacy NDC, 6 package rows | 20230805_58eaab62-ac36-4080-8ded-9b472dddc617.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-2131-8 | ML - Milliliter | 51672-2131 | 3ff51a3e-245f-4e75-a21e-7fe62e546dfd | 1 | 2018-02-20 |
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 |
|---|---|---|---|---|---|---|
| EMF | ARGENTUM NITRICUM, ARNICA MONTANA, BAPTISIA TINCTORIA, CINCHONA OFFICINALIS, GALIUM APARINE, HEPAR SUIS, NATRUM CARBONICUM, PANAX GINSENG, PHOSPHORICUM ACIDUM, PHOSPHORUS, RHODODENDRON CHRYSANTHUM, STRONTIUM CARBONICUM, SULPHUR IODATUM, THUJA OCCIDENTALIS, X-RAY | Liddell Laboratories, Inc. | 3fa1b8d3-7c09-431b-b843-03b2ef8a92b1 | 2024-07-01 | Warnings | E4GA8884NN |
| CHILDRENS LORATADINE | LORATADINE | TARGET CORPORATION | c5e87776-71e3-4c46-a8e7-30f47f437bef | 2024-06-28 | Warnings | 7AJO3BO7QN |
| Dye-Free Childrens Loratadine | LORATADINE | UP & UP | 85ea5c40-d02f-4c91-8eb2-4b16877e1eab | 2024-06-28 | Warnings | 7AJO3BO7QN |
| Loratadine | LORATADINE | WALGREEN CO. | c016aad8-df83-99b0-e053-2a95a90a49cf | 2024-06-24 | Warnings | 7AJO3BO7QN |
| Alavert Allergy | LORATADINE | Foundation Consumer Healthcare | 1704474a-9b99-de45-e063-6294a90ac59b | 2024-06-24 | Warnings | 7AJO3BO7QN |
| ABREVA Rapid Pain Relief | GLYCERIN, LIDOCAINE | Haleon US Holdings LLC | 65bd242f-4c6a-436c-8ec0-7b2e0d73ed9d | 2024-06-20 | Warnings | PDC6A3C0OX |
| Loratadine ODT | LORATADINE | WALGREEN CO. | 7556b959-3ff2-4489-ae06-67ef398c623c | 2024-06-18 | Warnings | 7AJO3BO7QN |
| All Day Allergy Relief | LORATADINE | QUALITY CHOICE (Chain Drug Marketing Association) | a282d209-1015-4570-b9df-7cc0a3753e37 | 2024-06-17 | Warnings | 7AJO3BO7QN |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Honeywell Safety Products USA, Inc. | ad42a7e3-84ea-390d-e053-2a95a90a3a32 | 2024-06-14 | Warnings | 059QF0KO0R |
| Loratadine | LORATADINE | Cardinal Health | c96dd1c9-85a0-0792-e053-2a95a90a2264 | 2024-06-14 | Warnings | 7AJO3BO7QN |
| MegaBabe Butt Stuff Hemorrhoidal | COCOA BUTTER, GLYCERIN, LIDOCAINE, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE | MEGABABE, LLC | 01c156ff-69f9-4d5e-a9ea-abbc52d4afff | 2024-06-12 | Warnings | PDC6A3C0OX |
| Loratadine | LORATADINE | NuCare Pharmaceuticals,Inc. | 6d0c0948-9288-9bb8-e053-2a91aa0abf3a | 2024-06-10 | Warnings | 692783 7AJO3BO7QN |
| PHOSPHORIC ACID | PHOSPHORIC ACID | Rxhomeo Private Limited d.b.a. Rxhomeo, Inc | 1a494ef4-89fd-92c2-e063-6394a90a7333 | 2024-06-07 | Warnings | E4GA8884NN |
| Eyes Alive Eye Wash | WATER | RIVIERA PHARMA INC | 081079f4-1c06-4054-b771-00fedaa666f6 | 2024-06-05 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Becton Dickinson and Company | 6e43c5a3-dad2-49ed-b500-964cb4563cc9 | 2024-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
| DNA Pancreas Formula | LYCOPODIUM CLAVATUM, PANCREATINUM, DNA, INSULINUM, PHOSPHORICUM ACIDUM, URANIUM NITRICUM, RADIUM BROMATUM | Nutritional Specialties, Inc. | 6abfbaab-71c4-45b1-9eb0-c42e8f0e0ff1 | 2024-05-29 | Warnings | E4GA8884NN |
| Jet Lag | ANACARDIUM ORIENTALE, APIS MELLIFICA, CARBO VEGETABILIS, CARDUUS MARIANUS, COCCULUS INDICUS, KALI PHOSPHORICUM, NUX VOMICA, PASSIFLORA INCARNATA, PHOSPHORICUM ACIDUM, TABACUM, | Liddell Laboratories, Inc. | 2bb38633-95a8-4db2-b4e8-8fc2fdbb5221 | 2024-05-20 | Warnings | E4GA8884NN |
| Allergy Relief | LORATADINE | QUALITY CHOICE (Chain Drug Marketing Association) | c5acd9d7-2f26-41c5-b369-2122251583ec | 2024-05-17 | Warnings | 7AJO3BO7QN |
| All Day Allergy Relief | LORATADINE | QUALITY CHOICE (Chain Drug Marketing Association) | d47a5f1b-fb27-4618-a26e-a5eeabcd87f2 | 2024-05-16 | Warnings | 7AJO3BO7QN |
| Sodium Phenylacetate and Sodium Benzoate | SODIUM PHENYLACETATE AND SODIUM BENZOATE | FOSUN PHARMA USA INC | cee1e9a2-bbe5-2419-e053-2a95a90ac3ef | 2024-05-09 | Warnings, Adverse reactions | OJ245FE5EU |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.