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 20 of 167 · 3,331 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pain ReliefMENTHOLShanghai Chuangshi Medical Technology (Group) Co., Ltd.3ed34e65-9d74-daff-e063-6394a90a94c72026-05-14WarningsExact identifier
unii: L7T10EIP3A
MENTHOL PAIN RELIEF Gel-PatchMENTHOLShanghai Chuangshi Medical Technology (Group) Co., Ltd.0e6a09cc-7986-f851-e063-6294a90aff672026-05-14WarningsExact identifier
unii: L7T10EIP3A
PAIN RELIEF Gel-PatchLIDOCAINE AND MENTHOLShanghai Chuangshi Medical Technology (Group) Co., Ltd.3c166165-2ad8-206f-e063-6294a90a52fc2026-05-14WarningsExact identifier
unii: L7T10EIP3A
OVERNIGHT RELIEF Gel-PatchMENTHOLShanghai Chuangshi Medical Technology (Group) Co., Ltd.f1041b25-eb09-e43d-e053-2995a90a073a2026-05-14WarningsExact identifier
unii: L7T10EIP3A
PAIN RELIEF Gel-PatchLIDOCAINE AND MENTHOLShanghai Chuangshi Medical Technology (Group) Co., Ltd.f1047707-3fe5-06bc-e053-2995a90a59b92026-05-14WarningsExact identifier
unii: L7T10EIP3A
Elastic Relief StripMENTHOLShanghai Chuangshi Medical Technology (Group) Co., Ltd.f103cf8a-a285-28d1-e053-2995a90ae70e2026-05-14WarningsExact identifier
unii: L7T10EIP3A
Halls Honey LemonMENTHOLMondelez Global LLCaec46410-ffb1-4db4-b232-82110c562f692026-05-13WarningsExact identifier
unii: L7T10EIP3A
Pain Relief Gel-Roll OnMENTHOLTrifecta Pharmaceuticals USA51b403dc-fc9b-0cad-e063-6394a90af0812026-05-13WarningsExact identifier
unii: L7T10EIP3A
BiofreezeMENTHOLReckitt Benckiser LLC5edddb99-6596-4a3b-b361-1cc04d032c312026-05-13WarningsExact identifier
unii: L7T10EIP3A
BiofreezeMENTHOLReckitt Benckiser LLC684faf63-5e44-4471-8384-e8fa7c0d842a2026-05-13WarningsExact identifier
unii: L7T10EIP3A
BiofreezeMENTHOLReckitt Benckiser LLC4c798b06-6ee5-41d1-8a14-f6889512ade32026-05-13WarningsExact identifier
unii: L7T10EIP3A
BIOFREEZEMENTHOLReckitt Benckiser LLC83d5c2f2-2413-4d28-83b2-0808d0917b4d2026-05-13WarningsExact identifier
unii: L7T10EIP3A
BiofreezeMENTHOLReckitt Benckiser LLC10a8face-47da-ebbe-e063-6294a90a42fe2026-05-13WarningsExact identifier
unii: L7T10EIP3A
Biofreeze Foot CreamMENTHOLReckitt Benckiser LLC32450cbf-4ed4-402b-a30e-e08a17bba3fb2026-05-13WarningsExact identifier
unii: L7T10EIP3A
BiofreezeMENTHOLReckitt Benckiser LLCa227213b-e89f-7144-e053-2a95a90a7e742026-05-13WarningsExact identifier
unii: L7T10EIP3A
BiofreezeMENTHOLReckitt Benckiser LLC00bb462a-27d0-6f74-e063-6394a90a90ec2026-05-13WarningsExact identifier
unii: L7T10EIP3A
BioFreeze Dry StickMENTHOLReckitt Benckiser LLC26d62cd2-9209-8cca-e063-6394a90a20282026-05-13WarningsExact identifier
unii: L7T10EIP3A
Biofreeze Colorless Roll-OnMENTHOLReckitt Benckiser LLCa8d59d45-0e85-43d1-affd-bbe922c4acb12026-05-13WarningsExact identifier
unii: L7T10EIP3A
Biofreeze ColorlessMENTHOLReckitt Benckiser LLC939dbbc3-71ec-4990-840e-7c9b8d4305622026-05-13WarningsExact identifier
unii: L7T10EIP3A
Biofreeze Flexible Relief StripMENTHOLReckitt Benckiser LLC6ec26bae-e395-49aa-969e-8c653d6f0b272026-05-13WarningsExact identifier
unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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