NDC 69580-784-54 - Green Compass Reduce Roll-On Pain Relief

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
69580-784
Requested NDC
69580-784-54
Package NDCs from labels
69580-784-54
Manufacturer
Royal Labs Natural Cosmetics, Inc.
Effective date
2021-01-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Green Compass Reduce Roll-On Pain ReliefRoyal Labs Natural Cosmetics, Inc.2021-01-16HUMAN 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 70 of 290 · 5,787 matching rows.

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Advanced Hand SanitizerETHYL ALCOHOLAmazon.Com Services LLC85421e9a-f1c9-4793-9479-8a072a610ed72026-03-03Warnings, Adverse reactionsExact identifier
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AntispeticEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLAmazon.com Services LLC7e628443-81b5-4728-b4c3-c02abecbdaa82026-03-03Warnings, Adverse reactionsExact identifier
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Aloe Vera GelLIDOCAINE HCL, MENTHOLAmazon.com Services LLC2acb1a6a-57e6-4915-b03a-89d1d2db3baf2026-03-03Warnings, Adverse reactionsExact identifier
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Pain ReliefARNICA MONTANA, BELLADONNA, GELSEMIUM SEMPERVIRENS, GNAPHALIUM POLYCEPHALUM, MAGNESIA PHOSPHORICA, SANGUINARIA CANADENSIS, SALIX ALBANaturalCare6eba2caa-958f-47a1-823c-c73bbb1d7fa92026-03-02WarningsExact identifier
unii: O80TY208ZW

Reported adverse events (FAERS/openFDA)#

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