NDC 83367-101-01 - Hoo Gargle Jasmine Mint Flavor

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
83367-101
Requested NDC
83367-101-01
Package NDCs from labels
83367-101-01, 83367-101-02, 83367-101-03, 83367-101-04, 83367-101-05, 83367-101-06, 83367-101-07, 83367-101-08
Manufacturer
Nuriearth Global Co., Ltd | Miko Co., Ltd.
Effective date
2023-04-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Hoo Gargle Jasmine Mint Flavor - Nuriearth Global Co., Ltd | Miko Co., Ltd.Nuriearth Global Co., Ltd | Miko Co., Ltd.2023-04-12HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83367-101-01Hoo Gargle Jasmine Mint Flavor15 mL in 1 PACKETLIQUID151
83367-101-02Hoo Gargle Jasmine Mint Flavor1 in 1 PACKAGELIQUID11
83367-101-03Hoo Gargle Jasmine Mint Flavor30 mL in 1 PACKETLIQUID301
83367-101-04Hoo Gargle Jasmine Mint Flavor1 in 1 PACKAGELIQUID11
83367-101-05Hoo Gargle Jasmine Mint Flavor50 mL in 1 PACKETLIQUID501
83367-101-06Hoo Gargle Jasmine Mint Flavor1 in 1 PACKAGELIQUID11
83367-101-07Hoo Gargle Jasmine Mint Flavor100 mL in 1 PACKETLIQUID1001
83367-101-08Hoo Gargle Jasmine Mint Flavor1 in 1 PACKAGELIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83367-101HOO GARGLE JASMINE MINT FLAVOR (SODIUM FLUORIDE) LIQUID [NURIEARTH GLOBAL CO., LTD]18 package rows20230413_f9298f43-04df-430c-e053-6294a90a9cb7.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 148 of 164 · 3,277 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NEUTRAMAXX 5000 TCPSODIUM FLUORIDEMassco Dental A Division of Dunagin Pharmaceuticalsf47cb584-eb8a-4297-ba32-5f435e85aacb2023-12-17WarningsExact identifier
unii: 8ZYQ1474W7
ORTHO GUARDSODIUM FLUORIDEMassco Dental A Division of Dunagin Pharmaceuticals8d3e0dd0-b584-413b-adf3-5c2d05ab72dd2023-12-17WarningsExact identifier
unii: 8ZYQ1474W7
NEUTRAMAXX 5000 PLUS TURBOSODIUM FLUORIDEMassco Dental A Division of Dunagin Pharmaceuticals3c7584f1-b652-4d82-99e7-10da0ee242c12023-12-17WarningsExact identifier
unii: 8ZYQ1474W7
NEUTRA MAXX 5000SODIUM FLUORIDEMassco Dental A Division of Dunagin Pharmaceuticalsfcbe6baa-2827-49df-9316-42cc865952032023-12-17WarningsExact identifier
unii: 8ZYQ1474W7
Hot/Cold Menthol 16% Roll-OnHOT/COLD MENTHOL 16% ROLL-ONHumco Holding Group, Inca8bf9744-9979-13c1-e053-2a95a90a30aa2023-12-15WarningsExact identifier
unii: L7T10EIP3A
BSSBALANCED SALT SOLUTIONAlcon Laboratories, Inc.28488c7b-cf6a-4a03-916f-cc66b3afdc572023-12-14Warnings, Adverse reactionsExact identifier
unii: 4550K0SC9B
Freds Medicated anti itchPRAMOXINE HYDROCHLORIDE, MENTHOLDiscount Drug Mart8697b932-da5a-717e-e053-2a91aa0afcae2023-12-12WarningsExact identifier
unii: L7T10EIP3A
CVS Medicated anti itchPRAMOXINE HYDROCHLORIDE, MENTHOLCVS86972218-31fe-6942-e053-2991aa0a88502023-12-12WarningsExact identifier
unii: L7T10EIP3A
Best Choice Medicated anti itchPRAMOXINE HYDROCHLORIDE, MENTHOLvalue merchandisers869631f8-aa1e-8ea4-e053-2a91aa0a5c572023-12-12WarningsExact identifier
unii: L7T10EIP3A
Moon Whitening Gel AnticavitySODIUM FLUORIDEMoon Oral Care, LLC0c556a29-a697-3a66-e063-6394a90abfee2023-12-12WarningsExact identifier
unii: 8ZYQ1474W7
Moon Charcoal Whitening AnticavitySODIUM FLUORIDEMoon Oral Care, LLC0c55f7b3-fea1-58f3-e063-6394a90a3bde2023-12-12WarningsExact identifier
unii: 8ZYQ1474W7
Ageless Pain ReliefMETHYL SALICYLATE, MENTHOLIsagenix International, LLC3c7e493b-923d-44b1-9076-46c7894308d42023-12-12Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
ORCA Complete Menthol Pain RelieverMENTHOLORCA Products, LLC99990e27-d66b-4d61-97f2-6a76066eb8b82023-12-08WarningsExact identifier
unii: L7T10EIP3A
Katinko External Analgesic OilCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATEGreenstone Pharmaceutical Inc.5881fc35-3293-4f0b-801a-afcd6feb94962023-12-08WarningsExact identifier
unii: L7T10EIP3A
Katinko Pain And Itch RelievingCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATEGreenstone Pharmaceutical Inc.fe907fa4-4a01-4974-b71f-9cd980b4eaa22023-12-08Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A
CycleMENTHOLLa Mend, Inc.cfc0bcde-ef91-1e6c-e053-2a95a90ab79e2023-12-07WarningsExact identifier
unii: L7T10EIP3A
Overnight Cold Therapy Pain ReliefMENTHOL, UNSPECIFIED FORMWalgreen Co.2cbd0966-4cf9-4271-bd53-6672b1ed2a992023-12-04WarningsExact identifier
unii: L7T10EIP3A
Liberdol Topical AnalgesicMETHYL SALICYLATE, MENTHOL, CAMPHOR (SYNTHETIC)ViaDerma Distribution, Incab52cd0e-34fa-41c7-9ce7-1183c2aff8d82023-12-01WarningsExact identifier
unii: L7T10EIP3A
Menthozen HydrogelMENTHOL, CAPSAICINProficient Rx LP85a7809e-c43f-4138-a85b-44e1b586def52023-12-01WarningsExact identifier
unii: L7T10EIP3A
Menthozen CreamMETHYL SALICYLATE, MENTHOL, CAPSAICINProficient Rx LP66681906-c5f5-4c57-bb43-9c83cccc00622023-12-01WarningsExact identifier
unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.