Home NDC 78151-060-01 NDC 78151-060-01 - Karl and Hans Botanic Jasmine 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 78151-060
Requested NDC 78151-060-01
Package NDCs from labels 78151-060-01, 78151-060-02
Manufacturer PIGEON CORPORATION | DONG IL PHARMS CO., LTD.
Effective date 2024-08-08
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Drug Facts PIGEON CORPORATION | DONG IL PHARMS CO., LTD. 2024-08-08 HUMAN OTC DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 78151-060-01 Karl and Hans Botanic Jasmine 120 g in 1 TUBE PASTE, DENTIFRICE 120 1 78151-060-02 Karl and Hans Botanic Jasmine 1 in 1 CARTON PASTE, DENTIFRICE 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 78151-060 KARL AND HANS BOTANIC JASMINE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [PIGEON CORPORATION] 1 Current NDC, 2 package rows 20240809_6c0335e6-f041-48c7-9da3-88c124b84b00.zip
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 47 of 73 · 1,449 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Tidalove COOL MINT TOOTHPASTE TABLETS Paranmare LLC 4093060c-23a5-c77a-e063-6394a90a9304 2025-10-07 Warnings Exact identifier application number: M021 Tidalove YUZU MINT TOOTHPASTE TABLETS Paranmare LLC 40946943-21cf-b114-e063-6394a90aed3f 2025-10-07 Warnings Exact identifier application number: M021 Optimax Purple Anticavity Fluoride SODIUM MONOFLUOROPHOSPHATE WHITE GLO USA INC fdb16e59-5be1-4bd0-a940-d542d67fb2df 2025-10-02 Warnings Exact identifier application number: M021 Xpect Industrial Eye Relief GLYCERIN, NAPHAZOLINE HCL Cintas Corporation a0167d06-7adb-36f4-e053-2a95a90af9ef 2025-09-30 Warnings Exact identifier unii: PDC6A3C0OX Intensive Enamel Repair Whitening TP INTENSIVE ENAMEL REPAIR WHITENING TP Topco Associates LLC 3012a8da-7595-2f7c-e063-6294a90ae120 2025-09-30 Warnings Exact identifier application number: M021 Made by Dentists For Kids Eyeball Juice (Watermelon) SODIUM FLUORIDE MADE BY DENTISTS INC b2ad2b19-6fdf-454d-9b1d-49b1c81016fd 2025-09-30 Warnings Exact identifier application number: M021 ACT Restoring Anticavity Fluoride Mint Burst SODIUM FLUORIDE Chattem, Inc. a38363e6-7105-4663-95a0-09ecb2948f83 2025-09-30 Warnings Exact identifier application number: M021 Xpect Eyewash EYEWASH Cintas Corporation 1d69365d-662b-4248-8fa9-1629451b549a 2025-09-30 Warnings Exact identifier unii: 059QF0KO0R CheBoho TEA TREE ACNE CHEBOHO TEA TREE ACNE Opalshi(Guangzhou)E-commerce Co. Ltd. 3fc4cf84-b2da-c593-e063-6394a90abc5c 2025-09-27 Warnings Exact identifier unii: 059QF0KO0R UNPA CHA CHA TOOTHPASTE SODIUM MONOFLUOROPHOSPHATE DONG IL PHARMS CO.,LTD 3fae966e-0246-b9f2-e063-6394a90a494c 2025-09-26 Warnings Exact identifier application number: M021 rxcui: 1737795 unii: C810JCZ56Q Cloveden Tooth SODIUM MONOFLUOROPHOSPHATE DONG IL PHARMS CO.,LTD 3fb01bea-7205-49ba-e063-6294a90a3841 2025-09-26 Warnings Exact identifier application number: M021 unii: C810JCZ56Q Cloveden Sensitive Care Tooth SODIUM FLUORIDE DONG IL PHARMS CO.,LTD 3fb153f1-ba6e-7251-e063-6294a90abe62 2025-09-26 Warnings Exact identifier application number: M021 Cloveden 100 times higher concentrated CETYLPYRIDINIUM CHLORIDE DONG IL PHARMS CO.,LTD 3fb1a2ee-381e-a9e8-e063-6394a90a864b 2025-09-26 Warnings Exact identifier application number: M021 unpa Cha Cha Toothpaste SODIUM MONOFLUOROPHOSPHATE Lycl Inc. 230b3cf2-053a-4e8b-8d50-05bbc877faa8 2025-09-25 Warnings Exact identifier application number: M021 rxcui: 1737795 unii: C810JCZ56Q Hemorrhoidal Pain Relief HEMORRHOIDAL PAIN RELIEF CREAM Neilmed Pharmaceuticals Inc. 374dc1c0-4243-b272-e063-6394a90a5a6b 2025-09-24 Warnings Exact identifier unii: PDC6A3C0OX TheraBreath Anticavity SODIUM FLUORIDE Church & Dwight Co., Inc. 3c5d58f1-ea8c-4708-bbc6-21e1cd1446da 2025-09-19 Warnings Exact identifier application number: M021 Sterile Water WATER ProPharma Distribution 3f2ae880-852f-b45d-e063-6394a90aa1cc 2025-09-19 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R Optimax Professional Whitening Anticavity Fluoride SODIUM MONOFLUOROPHOSPHATE WHITE GLO USA INC 8c4b9db9-8f23-4dd5-ab6e-1c2f9a3da5b1 2025-09-18 Warnings Exact identifier application number: M021 Optimax Professional Whitening Anticavity Fluoride SODIUM MONOFLUOROPHOSPHATE WHITE GLO USA INC c1bbdd36-53fb-43a3-ba20-afbeb6359d31 2025-09-18 Warnings Exact identifier application number: M021 REFRESH OPTIVE Drops CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN Allergan, Inc. 80275190-d717-40ea-905b-5c8fbe986eac 2025-09-15 Warnings Exact identifier unii: PDC6A3C0OX
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.