FDA.reportPublic FDA data

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#

NDC, Related label table
NDCRelated label
83367-101-02f9298f43-04df-430c-e053-6294a90a9cb7
83367-101-04f9298f43-04df-430c-e053-6294a90a9cb7
83367-101-06f9298f43-04df-430c-e053-6294a90a9cb7
83367-101-08f9298f43-04df-430c-e053-6294a90a9cb7

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 80 of 167 · 3,331 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MentholMAXIMUM STRENGTH MEDICATED FOOT POWDERVALU MERCHANDISERS, CO89a5c4bb-442f-d3f0-e053-2a95a90a51bd2025-11-24WarningsExact identifier
unii: L7T10EIP3A
Dragon Pain Relieving BalmCAMPHOR, MENTHOLAMERICANNA WELLNESS, INC.0d11ab8e-d3ea-c7ef-e063-6294a90ae0a32025-11-24WarningsExact identifier
unii: L7T10EIP3A
Dragon Pain RelievingCAMPHOR, MENTHOLAMERICANNA WELLNESS, INC.0d113dec-8832-d984-e063-6394a90ae7b32025-11-24WarningsExact identifier
unii: L7T10EIP3A
Dragon Pain Relieving BalmCAMPHOR, MENTHOLAMERICANNA WELLNESS, INC.0d12f03f-dd8b-0be5-e063-6294a90a43db2025-11-24WarningsExact identifier
unii: L7T10EIP3A
Dragon Pain Relieving BalmCAMPHOR, MENTHOLAMERICANNA WELLNESS, INC.0d129641-eaea-c3ee-e063-6394a90aa58f2025-11-24WarningsExact identifier
unii: L7T10EIP3A
Dragon Pain Relieving BalmCAMPHOR, MENTHOLAmericanna Wellness, Inc.002db658-6b1f-ea49-e063-6294a90ae3e72025-11-24WarningsExact identifier
unii: L7T10EIP3A
Sensodyne Cavity and SensitivityPOTASSIUM NITRATE, SODIUM FLUORIDEHaleon US Holdings LLCd002074b-0580-4247-b3c7-121b8c0986972025-11-24WarningsExact identifier
unii: 8ZYQ1474W7
Dragon Pain Relieving BalmCAMPHOR, MENTHOLAmericanna Wellness, Inc.002997d0-3176-3918-e063-6294a90a44082025-11-24WarningsExact identifier
unii: L7T10EIP3A
Dragon Pain RelievingCAMPHOR, MENTHOLAMERICANNA WELLNESS, INC.0d1059cc-1b0b-4e7b-e063-6294a90a56ea2025-11-24WarningsExact identifier
unii: L7T10EIP3A
GuruNanda Pain ReliefMENTHOL AND CAMPHORGURUNANDA, LLC3ca78342-cc6d-5f6b-e063-6294a90a3f1c2025-11-24WarningsExact identifier
unii: L7T10EIP3A
Dragon Pain RelievingCAMPHOR, MENTHOLAMERICANNA WELLNESS, INC.0d118256-90ee-28ef-e063-6394a90a21e82025-11-24WarningsExact identifier
unii: L7T10EIP3A
HEB Extra WhiteningFLUORIDEHEB9bdcbd3f-095b-43d1-8a8e-0ba3eab14e0e2025-11-21WarningsExact identifier
unii: 8ZYQ1474W7
HEB Enamel Protection Multi ActionPOTASSIUM NITRATE, SODIUM FLUORIDEHEB8255de83-aa60-b081-e053-2a91aa0afcdc2025-11-21WarningsExact identifier
unii: 8ZYQ1474W7
CVS Enamel GuardFLUORIDECVS Pharmacyd9dfa515-426b-9059-e053-2a95a90a38852025-11-21WarningsExact identifier
unii: 8ZYQ1474W7
CVS Pharmacy Enamel GuardFLUORIDECVS Pharmacy18295a1c-c2a6-489b-be34-9252b9e1e2b82025-11-21WarningsExact identifier
unii: 8ZYQ1474W7
CVS Extra WhiteningFLUORIDECVS Pharmacy3b019849-6585-4a8c-a90a-c7e9e617b3ef2025-11-21WarningsExact identifier
unii: 8ZYQ1474W7
DG 4x Medicated Tooth and Gum CreamBENZOCAINEDollar Generalb2c156f0-6d11-1eba-e053-2995a90a6db82025-11-21WarningsExact identifier
unii: L7T10EIP3A
4x Medicated Toothache and Gum GelBENZOCAINECVSa7577d5f-69cf-3f32-e053-2995a90aaba52025-11-21WarningsExact identifier
unii: L7T10EIP3A
Walgreens Sensitive Extra WhiteningSODIUM FLUORIDEWalgreense807b8a0-6d58-a15f-e053-2995a90a2ea12025-11-21WarningsExact identifier
unii: 8ZYQ1474W7
Toothache and Gum Relief CushionsBENZOCAINERite Aid9970d485-0b78-1438-e053-2995a90ad32c2025-11-21WarningsExact identifier
unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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