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 |
|---|---|---|---|---|---|---|
| RPT-Sys | EMOTIONAL REBALANCE | Vitality Works, Inc. | 0e8768fe-c2ba-41e9-93ac-c142fae6e879 | 2025-12-17 | Warnings | E4GA8884NN |
| Woman Power | AGNUS, ARALIA QUIN, ARNICA, DAMIANA, LACTUCA, NAT MUR, ONOSMODIUM VIRGINIANUM, OOPHORINUM, PHOSPHORICUM AC, PITUITARUM POSTERIUM, SALIX NIG, SEPIA, THUJA OCC | Eight and Company L.L.C | 614d47de-742b-4944-89c8-59f2f58dc8b9 | 2025-12-17 | Warnings | E4GA8884NN |
| STERILE CORD BLOOD COLLECTION UNIT (MSC123D) | ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE | Maco Productions | e3b456ec-4578-485f-a696-8a343505f30b | 2025-12-16 | Warnings | 5QWK665956 |
| Mood | ARALIA QUIN, CIMICIFUGA, SPIGELIA ANTH, ARG NIT, ARSENICUM ALB, AURUM MET, IGNATIA AMARA, LACHESIS, LYCOPODIUM, NAT MUR, PHOSPHORICUM AC, PLATINUM MET, PULSATILLA, SEPIA, THUJA OCC | Natural Creations, Inc | 7f143f30-2b72-4e6c-985c-8d3a485dbdb4 | 2025-12-16 | Warnings | E4GA8884NN |
| Panacode | SYZYGIUM, HYDRASTIS, ADRENALINUM, PANCREATINUM, PITUITARUM POSTERIUM, BOVISTA, INSULIN, LYCOPERSICUM, PHOSPHORICUM AC, PHOSPHORUS, TARENTULA HISPANA, TEREBINTHINA, URANIUM NITRICUM | Natural Creations, Inc | f2144c14-28a2-4dc4-b517-0f81e9c8b720 | 2025-12-16 | Warnings | E4GA8884NN |
| Chronic Fatigue Therapy | EPINEPHRINE, GOLD, CHELIDONIUM MAJUS, ECHINACEA, GINKGO, HELLEBORUS NIGER, PHOSPHORIC ACID, SCUTELLARIA LATERIFLORA, THUJA OCCIDENTALIS | TRP Company | 751334b8-f21b-3f94-e053-2a91aa0a9bb9 | 2025-12-15 | Warnings | E4GA8884NN |
| Artificial Tears | GLYCERIN | NuCare Pharmaceuticals,Inc. | 97a3d8e2-b2c0-3f5d-e053-2a95a90ac49d | 2025-12-15 | Warnings | PDC6A3C0OX |
| ElixirLidoFast Rapid Relief | GLYCERIN, LIDOCAINE, PETROLATUM, AND PHENYLEPHRINE HYDROCHLORIDE | ELIXIR HEALTHCARE USA, LLC. | 45de9dfa-6c89-1eae-e063-6294a90a4dac | 2025-12-13 | Warnings | PDC6A3C0OX |
| Allergy Relief | LORATADINE | Valu Merchandisers Company | 05927511-6b7a-4e29-96b4-3043493acf11 | 2025-12-11 | Warnings | 7AJO3BO7QN |
| Kroger Hemorrhoid | GLYCERIN, LIDOCAINE, PETROLATUM, PHENYLEPHRINE HCL | Kroger Company | 45b2dd86-7fb0-07bf-e063-6394a90a1884 | 2025-12-11 | Warnings | PDC6A3C0OX |
| Firstep Firstflush | EYEWASH | Encon Safety Products, Inc. | a44beb26-79ae-98bd-e053-2995a90a9b74 | 2025-12-09 | Warnings | 059QF0KO0R |
| Loratadine | LORATADINE | Major Pharmaceuticals | dee25423-377b-4b94-a4a8-0dfb8f51aaab | 2025-12-08 | Warnings | 7AJO3BO7QN |
| Sodium phenylacetate and Sodium benzoate | SODIUM PHENYLACETATE AND SODIUM BENZOATE | Navinta LLC | d20768fe-4516-483a-a082-ff1df9ad1d99 | 2025-12-06 | Warnings, Adverse reactions | OJ245FE5EU |
| Loratadine antihistamine | LORATADINE | A-S Medication Solutions | 1203981a-becd-4854-810d-b6d8842b5bd2 | 2025-12-06 | Warnings | 7AJO3BO7QN |
| Claritin | LORATADINE | Bayer HealthCare LLC. | 660ac9df-f1b1-4c89-94dd-9fae0a013f3c | 2025-12-05 | Warnings | 7AJO3BO7QN |
| Claritin Reditabs | LORATADINE | Bayer Healthcare LLC. | b681ea25-d00b-4c8a-8054-cc6f983ce337 | 2025-12-05 | Warnings | 7AJO3BO7QN |
| Claritin | LORATADINE | Bayer HealthCare LLC. | 37732ca2-b454-4215-91a2-c62e0f7a56af | 2025-12-05 | Warnings | 7AJO3BO7QN |
| Claritin-D 24 Hour | LORATADINE AND PSEUDOEPHEDRINE SULFATE | Bayer HealthCare LLC. | f046a807-ab8c-0620-e053-2a95a90a9d3c | 2025-12-05 | Warnings | 7AJO3BO7QN |
| Claritin | LORATADINE | Bayer HealthCare LLC. | 20938e05-bc3e-51aa-e054-00144ff88e88 | 2025-12-05 | 7AJO3BO7QN | |
| Claritin Chewable Cool Mint Flavor | LORATADINE | Bayer HealthCare LLC. | 98b99bb9-d499-9ab4-e053-2a95a90a6ae6 | 2025-12-05 | Warnings | 7AJO3BO7QN |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.