Home NDC 83062-030 NDC 83062-030 - DuoCare Clinical Oral Rinse 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 83062-030
Package NDCs from labels 83062-030-13, 83062-030-07
Manufacturer IIMED MEDICAL MEXICANA S DE RL DE CV | Team Technologies
Effective date 2023-10-20
Current FDA listing Not matched in FDA.report NDC product tables
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 70 of 93 · 1,848 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Topicale Xtra BENZOCAINE Medical Products Laboratories,Inc. e3da0e63-a891-72bd-e053-2a95a90a58bc 2024-12-11 Warnings Exact identifier application number: M022 Topicale Xtra BENZOCAINE Medical Products Laboratories, Inc. e3d924b5-0788-46d3-e053-2995a90a027b 2024-12-11 Warnings Exact identifier application number: M022 CVS Muscle Rub MENTHOL 10%, METHYL SALICYLATE 15% CVS Health c72c9a95-4226-6d69-e053-2a95a90a8e1c 2024-12-11 Warnings Exact identifier unii: LAV5U5022Y Fluoride Bits SODIUM MONOFLUOROPHOSPHATE 0.76% The Kind Lab, Inc. fa433031-7376-0e5b-e053-6394a90a5f75 2024-12-11 Warnings Exact identifier application number: M022 Fluoride Bits SODIUM MONOFLUOROPHOSPHATE 0.76% The Kind Lab, Inc. eedf13dc-a009-027a-e053-2995a90a8ec8 2024-12-11 Warnings Exact identifier application number: M022 BENGAY ULTRA STRENGTH NON-GREASY CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE Kenvue Brands LLC 0a41ec65-bd0b-4fc6-807d-74f353341cc7 2024-12-11 Warnings Exact identifier unii: LAV5U5022Y Equate Healthy Gums Clean Mint Breath Oral Rinse CETYLPYRIDINIUM CHLORIDE Vasu Healthcare Pvt. Ltd. 05fc922a-73fc-4826-be77-538da08282b9 2024-12-11 Warnings Exact identifier unii: D9OM4SK49P Fendall Pure Flow PURIFIED WATER Honeywell Safety Products USA, Inc. afda6fc3-7615-b0be-e053-2995a90a6208 2024-12-10 Warnings Exact identifier unii: 059QF0KO0R NATURAL LEMON MINT HERB THROAT DROPS MENTHOL Ricola USA Inc. 763e8234-60be-4b1f-9f78-01c574f35d0a 2024-12-10 Warnings Exact identifier application number: M022 Natural Cherry Honey Herb Throat Drops MENTHOL Ricola USA Inc. 989f8509-cd28-48e7-9aa1-baddfbcac95a 2024-12-10 Warnings Exact identifier application number: M022 ORGANIC PEPPERMINT HERB THROAT DROPS MENTHOL Ricola USA Inc. f75c8967-40e6-473a-b403-941354cb0be1 2024-12-10 Warnings Exact identifier application number: M022 Natural Cherry Honey Herb Throat Drops MENTHOL Ricola USA Inc. c56be34d-1dd5-4200-9723-3a73180cb759 2024-12-10 Warnings Exact identifier application number: M022 Cherry Throat Drops MENTHOL Ricola USA Inc. 89257ceb-af0f-4516-88f7-6dfdab9e14f4 2024-12-10 Warnings Exact identifier application number: M022 BERRY MEDLEY THROAT DROPS MENTHOL Ricola USA Inc. 9bfd2ea7-745b-47f8-bd8a-9dbeeaad8b95 2024-12-10 Warnings Exact identifier application number: M022 NATURAL LEMON MINT HERB THROAT DROPS MENTHOL Ricola USA Inc. 6a81e5c7-834d-44da-853f-8f6103236311 2024-12-10 Warnings Exact identifier application number: M022 SUGAR FREE SWISS CHERRY HERB THROAT DROPS MENTHOL Ricola USA Inc. 8a24f614-8e21-4ab2-8c0e-6af947911ccd 2024-12-10 Warnings Exact identifier application number: M022 RICOLA MAX NASAL CARE COOL MENTHOL MENTHOL Ricola USA Inc. a2e189a2-65ae-48a9-99ad-8795334082df 2024-12-10 Warnings Exact identifier application number: M022 COOL RELIEF LEMON FROST ORAL ANESTHETIC MENTHOL Ricola USA Inc. 40c3a80a-a116-4607-bb4a-c89d255ee076 2024-12-10 Warnings Exact identifier application number: M022 COOL RELIEF ORAL ANESTHETIC MENTHOL Ricola USA Inc. d66f47a9-35ab-4bf9-8065-c81abcb503f5 2024-12-10 Warnings Exact identifier application number: M022 Natural Cherry Honey Herb Throat Drops MENTHOL Ricola USA Inc. 62a631d3-e6d0-4fca-ad0c-7c1b67d2a827 2024-12-10 Warnings Exact identifier application number: M022
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.