NDC 51672-2141-01 - Childrens Fexofenadine Hydrochloride Allergy
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
- 51672-2141
- Requested NDC
- 51672-2141-01
- Package NDCs from labels
- 51672-2141-8, 51672-2141-1, 51672-2141-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd.
- Effective date
- 2026-08-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Children's Fexofenadine Hcl Allergy | Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd. | 2026-08-11 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-2141-1 | Childrens Fexofenadine HydrochlorideAllergy | 1 in 1 CARTON | SUSPENSION | 1 | 5 | |
| 51672-2141-1 | Childrens Fexofenadine HydrochlorideAllergy | 240 mL in 1 BOTTLE | SUSPENSION | 240 | 5 | |
| 51672-2141-8 | Childrens Fexofenadine HydrochlorideAllergy | 120 mL in 1 BOTTLE | SUSPENSION | 120 | 5 | |
| 51672-2141-8 | Childrens Fexofenadine HydrochlorideAllergy | 1 in 1 CARTON | SUSPENSION | 1 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-2141 | CHILDRENS FEXOFENADINE HYDROCHLORIDE ALLERGY (FEXOFENADINE HYDROCHLORIDE) SUSPENSION [TARO PHARMACEUTICALS U.S.A., INC.] | 3 | Current NDC, 4 package rows | 20240130_b21bb11d-bf74-4ee7-9cfe-5b599a3c4775.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-2141-8 | ML - Milliliter | 51672-2141 | 7cefccf4-e5bd-46d0-9216-72503db97050 | 1 | 2026-04-20 |
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.
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| BM Nat Phos | NATRUM PHOSPHORICUM | Total Operations Management LLC DBA:Bestmade Natural Products Micro | 53bacdaf-d7c8-9ae9-e063-6294a90a898c | 2026-06-08 | Warnings | 70WT22SF4B |
| Scrofularoforce | RUMEX CRISPUS, XANTHOXYLUM FRAXINEUM, LYMPH NODE (SUIS), SCROPHULARIA NODOSA, BARYTA CARBONICA, BARYTA MURIATICA, BELLADONNA, CALCAREA CARBONICA, CONIUM MACULATUM, HELLEBORUS NIGER, IODIUM, KALI PHOSPHORICUM, LACHESIS MUTUS, NATRUM PHOSPHORICUM, SILICEA, JUNIPERUS VIRGINIANA | BioActive Nutritional, Inc. | 737cd410-0405-41b0-b7f2-29bb20037849 | 2026-06-08 | Warnings | 70WT22SF4B |
| Allergy Relief | FEXOFENADINE HCL | P & L Development, LLC | a976ad95-33d2-49f5-bad5-e980bf764879 | 2026-06-08 | Warnings | 2S068B75ZU |
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| Eryfotona Actinica Tinted | TITANIUM DIOXIDE | ISDIN Corp. | 97357703-0e93-4216-bd1b-a9b202781959 | 2026-06-05 | Warnings | 15FIX9V2JP |
| Mineral Mattescreen SPF 40 - Untinted | TITANIUM DIOXIDE, ZINC OXIDE | Supergoop, LLC | 08671d39-3be2-d666-e063-6294a90a6207 | 2026-06-04 | Warnings | 15FIX9V2JP |
| Mineral Mattescreen SPF 40 - Golden Hour | TITANIUM DIOXIDE, ZINC OXIDE | Supergoop, LLC | c2398820-f003-707f-e053-2a95a90a6929 | 2026-06-04 | Warnings | 15FIX9V2JP |
| Epionce Daily Shield Tinted SPF 50 | TITANIUM DIOXIDE, ZINC OXIDE | Episciences, Inc. | 3d1e2921-cba9-4446-e054-00144ff8d46c | 2026-06-04 | Warnings | 15FIX9V2JP |
| ANESSA PERFECT UV SUNSCREEN SKINCARE MILK GB | ZINC OXIDE OCTOCRYLENE ETHYLHEXYL SALICYLATE HOMOSALATE TITANIUM DIOXIDE | HONGKONG JIAHE INTERNATIONAL HOLDING LIMITED | 5354af18-50c4-5fba-e063-6394a90ace39 | 2026-06-03 | Warnings | 15FIX9V2JP |
| BM Nat Phos Icing Sugar | NATRUM PHOSPHORICUM ICING SUGAR | Total Operations Management LLC DBA:Bestmade Natural Products Micro | 5356e3a2-11f9-98e5-e063-6294a90a08eb | 2026-06-03 | Warnings | 70WT22SF4B |
| ATOMY BB SUNSCREEN | TITANIUM DIOXIDE, ZINC OXIDE | ATOMY CO., LTD. | b0cd27ee-4917-4800-bcdf-c6e14b28c1d1 | 2026-06-02 | Warnings | 15FIX9V2JP |
| Atomy Sunscreen White Broad Spectrum SPF 50 PLUS | HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE | ATOMY CO., LTD. | ad0b9091-a990-45bf-93f4-d886be1bbffe | 2026-06-02 | Warnings | 15FIX9V2JP |
| Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUS | HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE | ATOMY CO., LTD. | 994d5680-284e-4faf-a29b-4d28f8d46e8f | 2026-06-02 | Warnings | 15FIX9V2JP |
| Matte Veil Tinted Broad Spectrum Sunscreen SPF 40 | ZINC OXIDE, TITANIUM DIOXIDE | Private Label Skin Care | a8d60212-18a7-42af-8bb3-bfcff7690a49 | 2026-06-02 | Warnings | 15FIX9V2JP |
| The Mineral Melt SPF30 | ZINC OXIDE, TITANIUM DIOXIDE | Dune Suncare Inc. | 2114fc3b-c8ce-45d2-8a82-4dc54f0adaf3 | 2026-06-02 | Warnings | 15FIX9V2JP |
| LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS UV AIR MINERAL SERUM SUNSCREEN BROAD SPECTRUM SPF 50 | TITANIUM DIOXIDE AND ZINC OXIDE | LOreal USA Products Inc | a1acb789-5bf4-4447-b3c5-4a7d4d3013a7 | 2026-06-01 | Warnings | 15FIX9V2JP |
| Allegra Allergy 24 hour | FEXOFENADINE HYDROCHLORIDE | Select Consumer Group | 2de81a41-8488-7e39-e063-6294a90a394b | 2026-06-01 | Warnings | 2S068B75ZU |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.