FDA.reportPublic FDA data

NDC 83702-005-11 - Rotosxika Lumbat Vertebra Plaster

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
83702-005
Requested NDC
83702-005-11
Package NDCs from labels
83702-005-11, 83702-005-12
Manufacturer
Puning Xinhua Trade Co., Ltd. | Nanyang Jingzhilan Biotechnology Co., Ltd.
Effective date
2023-09-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Rotosxika Lumbat Vertebra PlasterPuning Xinhua Trade Co., Ltd. | Nanyang Jingzhilan Biotechnology Co., Ltd.2023-09-21HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83702-005-122025-01-30C16284748780-12cef2736-5a17-d83d-e063-dadaa90ab31f05ea9eea-3d6a-3778-e063-6294a90ad8ac

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83702-005-11Rotosxika wormwood cervical patch2.1 g in 1 PATCHPATCH2.11
83702-005-12Rotosxika wormwood cervical patch12 in 1 BAGPATCH121

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83702-005ROTOSXIKA LUMBAT VERTEBRA PLASTER (MENTHOL, CAMPHOR) PATCH ROTOSXIKA KNEE PLASTER (MENTHOL, CAMPHOR) PATCH ROTOSXIKA HERBAL PAIN PATCH (MENTHOL, CAMPHOR) PATCH XINHUAZHX KNEE PLASTER (MENTHOL, CAMPHOR) PATCH XINHUAZHX WORMWOOD CERVICAL PATCH (MENTHOL, CAMPHOR) PATCH XINHUAZHX LUMBAT VERTEBRA PLASTER (MENTHOL, CAMPHOR) PATCH ROTOSXIKA WORMWOOD CERVICAL PATCH (MENTHOL, CAMPHOR) PATCH ROTOSXIKA SHOULDER PAIN PLASTER (MENTHOL, CAMPHOR) PATCH XINHUAZHX SHOULDER PAIN PLASTER (MENTHOL, CAMPHOR) PATCH [PUNING XINHUA TRADE CO., LTD.]12 package rows20231008_05ea9eea-3d6a-3778-e063-6294a90ad8ac.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 13 of 122 · 2,428 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PAIN RELIEF Gel-PatchLIDOCAINE AND MENTHOLShanghai Chuangshi Medical Technology (Group) Co., Ltd.4fdae0ab-94ba-5707-e063-6294a90a1f9d2026-05-14WarningsExact identifier
unii: L7T10EIP3A
OVERNIGHT RELIEF Gel-PatchMENTHOLShanghai Chuangshi Medical Technology (Group) Co., Ltd.2c6c4737-dff3-6382-e063-6294a90a412c2026-05-14WarningsExact identifier
unii: L7T10EIP3A
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

Reported adverse events (FAERS/openFDA)#

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