NDC 84067-460 - Cream

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
84067-460
Package NDCs from labels
84067-460-01
Manufacturer
Shantou Youjia E-Commerce Co., Ltd.
Effective date
2024-03-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
SOUTH MOON Bunion Pain Relief CreamShantou Youjia E-Commerce Co., Ltd.2024-03-16HUMAN OTC DRUG LABEL

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 3 of 3 · 44 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sumifun Knee Relieve PatchKNEE RELIEVE PATCHZhengzhou Miaoqi Pharmaceutical Technology Co., Ltd0e031aa5-edf4-8c9d-e063-6394a90afee32024-01-02WarningsExact identifier
unii: M89NIB437X
YOBISINREHMANNIA ROOT, ANGELICA GIGAS ROOTLydia Co., Ltd.873ef769-6051-4914-e053-2a95a90a9edb2023-12-16WarningsExact identifier
unii: 1BEM3U6LQQ
CO COOLMENTHOL, PEPPERMINT OIL, PINUS PUMILIO BRANCH/LEAF OILLydia Co., Ltd.90b213fe-f7b9-555c-e053-2a95a90a1df32021-06-27WarningsExact identifier
unii: AV092KU4JH
Eagle Brand Medicated Roll On RefreshCAMPHOR, MENTHOLBorden Company (Private) Limited567b6820-fb52-630e-e063-6294a90a8bf82015-07-01WarningsExact identifier
unii: AV092KU4JH

Reported adverse events (FAERS/openFDA)#

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