Home NDC 51672-2085-01 NDC 51672-2085-01 - Childrens Loratadine 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 51672-2085
Requested NDC 51672-2085-01
Package NDCs from labels 51672-2085-8, 51672-2085-4, 51672-2085-5, 51672-2085-1, 51672-2085-01
Manufacturer Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd.
Effective date 2026-07-14
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51672-2085-1 Childrens Loratadine 1 in 1 CARTON SOLUTION 1 4 51672-2085-1 Childrens Loratadine 240 mL in 1 BOTTLE SOLUTION 240 4 51672-2085-4 Childrens Loratadine 1 in 1 CARTON SOLUTION 1 4 51672-2085-4 Childrens Loratadine 60 mL in 1 BOTTLE SOLUTION 60 4 51672-2085-5 Childrens Loratadine 180 mL in 1 BOTTLE SOLUTION 180 4 51672-2085-5 Childrens Loratadine 1 in 1 CARTON SOLUTION 1 4 51672-2085-8 Childrens Loratadine 120 mL in 1 BOTTLE SOLUTION 120 4 51672-2085-8 Childrens Loratadine 1 in 1 CARTON SOLUTION 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51672-2085 CHILDRENS LORATADINE (LORATADINE) SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.] 4 Current NDC, Legacy NDC, 8 package rows 20241222_12c8066a-3429-481e-b63a-7ea2b439a170.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Loratadine ACTIVE INGREDIENT 7AJO3BO7QN CHILDRENS LORATADINE (LORATADINE) SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.] 2 Loratadine ACTIVE MOIETY 7AJO3BO7QN CHILDRENS LORATADINE (LORATADINE) SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.] 2 citric acid monohydrate INACTIVE INGREDIENT 2968PHW8QP CHILDRENS LORATADINE (LORATADINE) SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.] 2 glycerin INACTIVE INGREDIENT PDC6A3C0OX CHILDRENS LORATADINE (LORATADINE) SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.] 2 propylene glycol INACTIVE INGREDIENT 6DC9Q167V3 CHILDRENS LORATADINE (LORATADINE) SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.] 2 sodium benzoate INACTIVE INGREDIENT OJ245FE5EU CHILDRENS LORATADINE (LORATADINE) SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.] 2 sodium metabisulfite INACTIVE INGREDIENT 4VON5FNS3C CHILDRENS LORATADINE (LORATADINE) SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.] 2 sucrose INACTIVE INGREDIENT C151H8M554 CHILDRENS LORATADINE (LORATADINE) SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.] 2 water INACTIVE INGREDIENT 059QF0KO0R CHILDRENS LORATADINE (LORATADINE) SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.] 2 LORATADINE ACTIVE INGREDIENT 7AJO3BO7QN CHILDRENS LORATADINE (LORATADINE) SOLUTION [AIDAREX PHARMACEUTICALS LLC] 1 LORATADINE ACTIVE MOIETY 7AJO3BO7QN CHILDRENS LORATADINE (LORATADINE) SOLUTION [AIDAREX PHARMACEUTICALS LLC] 1 CITRIC ACID MONOHYDRATE INACTIVE INGREDIENT 2968PHW8QP CHILDRENS LORATADINE (LORATADINE) SOLUTION [AIDAREX PHARMACEUTICALS LLC] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX CHILDRENS LORATADINE (LORATADINE) SOLUTION [AIDAREX PHARMACEUTICALS LLC] 1 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 CHILDRENS LORATADINE (LORATADINE) SOLUTION [AIDAREX PHARMACEUTICALS LLC] 1 SODIUM BENZOATE INACTIVE INGREDIENT OJ245FE5EU CHILDRENS LORATADINE (LORATADINE) SOLUTION [AIDAREX PHARMACEUTICALS LLC] 1 SODIUM METABISULFITE INACTIVE INGREDIENT 4VON5FNS3C CHILDRENS LORATADINE (LORATADINE) SOLUTION [AIDAREX PHARMACEUTICALS LLC] 1 SUCROSE INACTIVE INGREDIENT C151H8M554 CHILDRENS LORATADINE (LORATADINE) SOLUTION [AIDAREX PHARMACEUTICALS LLC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R CHILDRENS LORATADINE (LORATADINE) SOLUTION [AIDAREX PHARMACEUTICALS LLC] 1
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 46 of 52 · 1,025 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Loratadine ODT LORATADINE Wal-Mart Stores, Inc. f399f7ab-ab51-46ff-bce9-3014eb021930 2022-11-04 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine ODT LORATADINE Aurohealth LLC 1ba8e521-0b0f-419c-b7c3-fa9586f83f36 2022-11-03 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine ODT LORATADINE Aurohealth LLC 9f44382f-c289-402d-bb98-ec5fa80fc25d 2022-11-03 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine ODT LORATADINE Aurohealth LLC 8c119b12-f512-4207-b354-7244d1f9963a 2022-11-03 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE Aurohealth LLC 839e2e03-9ebb-4a44-b753-fb174bd36115 2022-11-03 Warnings Exact identifier unii: 7AJO3BO7QN Sterile Water WATER Fresenius Kabi USA, LLC b45e9f1d-9c48-4b46-8541-d846b89540df 2022-10-26 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R basic care allergy relief LORATADINE Amazon.com Services LLC a4a7f024-972b-4a16-9cb8-28954c2a74c6 2022-10-18 Warnings Exact identifier unii: 7AJO3BO7QN Eye wash PURIFIED WATER McKesson bd089fde-24ba-4de5-e053-2995a90a39bb 2022-10-18 Warnings Exact identifier unii: 059QF0KO0R dg health allergy relief LORATADINE Dolgencorp, LLC 04258018-3d57-46d7-9595-04786da3f51a 2022-10-13 Warnings Exact identifier unii: 7AJO3BO7QN Bach Original Flower Remedies Rock Water WATER Nelson Bach USA Limited ea242559-1618-3354-e053-2a95a90a1a95 2022-10-03 Warnings Exact identifier unii: 059QF0KO0R welby childrens allergy relief LORATADINE Aldi Inc 402c635d-4116-4767-baa9-e956fed02884 2022-09-26 Warnings Exact identifier rxcui: 692783 unii: 7AJO3BO7QN REFRESH OPTIVE CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN Allergan, Inc. 7f8d88af-fd3b-4138-af61-f24c59ccebd7 2022-09-23 Warnings Exact identifier unii: PDC6A3C0OX Sterile Water WATER Medical Purchasing Solutions, LLC e90b47e3-9636-b9ee-e053-2a95a90ad48c 2022-09-19 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R REFRESH OPTIVE Advanced CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80 Allergan, Inc. ebd0839e-2e1d-4e0e-986c-19f1f5c76358 2022-09-15 Warnings Exact identifier unii: PDC6A3C0OX REFRESH OPTIVE Advanced CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, AND POLYSORBATE 80 Allergan, Inc. aaa943e4-7c38-4c5a-b7c0-5a656d8cafc0 2022-09-01 Warnings Exact identifier unii: PDC6A3C0OX Loratadine LORATADINE Winco Foods, LLC. 2a6cf697-0084-4522-bc89-b3e0f96a598d 2022-08-17 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE WALGREENS CO. 71adc5b3-3a91-4a1f-acb3-78922a7d9d5a 2022-08-09 Warnings Exact identifier unii: 7AJO3BO7QN Glycerinum GLYCERINUM Hahnemann Laboratories, INC. e34f8796-85b5-2946-e053-2995a90a251e 2022-07-08 Exact identifier unii: PDC6A3C0OX REFRESH Optive Mega-3 CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80 Allergan, Inc. c5f2b3f2-2071-45bd-a010-67f848bc0233 2022-06-30 Warnings Exact identifier unii: PDC6A3C0OX Sterile Water WATER Fresenius Kabi USA, LLC f42ac50f-0ec5-4713-a4c8-99d972d90bed 2022-06-22 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.