FOOT DETOX

Manufacturer
Sichuan Fragrant Plant Biotechnology Co, Ltd
Effective date
2020-01-17
Label type
HUMAN OTC DRUG LABEL
Version
32589
Source
full-release
Hydrated at
2026-05-31 23:02:57

Label at a glance#

ProductFOOT DETOX
Active ingredientZINC OXIDE
Label structure13 sections

Dosage and administration

Adults, and children 12 years of age and over, clean and dry up the area for the patch to be attached. Remove the protective cover sheet and gently apply. Leave it on at least 4 hours before removal. Children under 12 years of age, consult a doctor.

Storage and handling

Store in a dry and cool place away from direct sunlight.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide    8.3%

Purpose

OTC - PURPOSE SECTION

Zinc Oxide                 Skin Protectant

Directions

INDICATIONS & USAGE SECTION

Adults, and children 12 years of age and over, clean and dry up the area for the patch to be attached. Remove the protective cover sheet and gently apply. Leave it on at least 4 hours before removal. Children under 12 years of age, consult a doctor.

DOSAGE & ADMINISTRATION SECTION

For adults, and children 12 years of age and over, use 1 patch daily before bed.

When Using the Product

OTC - WHEN USING SECTION

Do not use otherwise than directed.
Do not stretch out the adhesive tape.
Do not take out the contents from the patch.
If patch is damaged, discard it right away.

Warning

WARNINGS SECTION

For External Use Only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center right away.

Do Not Use

OTC - DO NOT USE SECTION

On wounds, damaged skin or face.
If you are allergic to any ingredients of the product.
With other external product at the same time.

Stop Use and Ask a Doctor

OTC - STOP USE SECTION

If allergic reaction or irritation occurs.
If you are pregnant, nursing or under medical treatment.

Storage

STORAGE AND HANDLING SECTION

Store in a dry and cool place away from direct sunlight.

Manufactured by

SPL UNCLASSIFIED SECTION

Sichuan Fragrant Plant Biotechnology Co, Ltd

Shigao Industrial Park, Tianfu New District, Xinjia Village, Shigao Town, Renshou County, Chengdu, Sichuan, China 610020

Phone: 86-28-83503710

Inactive Ingredients

INACTIVE INGREDIENT SECTION

FERRIC OXIDE RED, APPLE CIDER VINEGAR, SHRIMP SHELL CHITIN, SCHORL TOURMALINE, POLYETHYLENE GLYCOL 200, PANAX NOTOGINSENG ROOT, SALVIA MILTIORRHIZA ROOT, HIPPOPHAE RHAMNOIDES FRUIT, GYNOSTEMMA PENTAPHYLLUM LEAF

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70837-001-012022-01-28C16284748780-1d6a99b39-3788-a426-e053-dadaa90af4c2Sichuan Fragrant Plant Biotechnology Co, Ltd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70837-001-01FOOT DETOX100 g in 1 PATCHPATCH10032589
70837-001-01FOOT DETOX30 in 1 BOXPATCH3032589

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70837-001FOOT DETOX (ZINC OXIDE) PATCH [SICHUAN FRAGRANT PLANT BIOTECHNOLOGY CO, LTD]32589Legacy NDC, 2 package rows20200118_06c855f9-9de2-4844-a726-73169a4724e9.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70837-00170837-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0ef21054-cb7e-42a5-93c5-c817f2de184706c855f9-9de2-4844-a726-73169a4724e92020-01-17WarningsExact identifier
spl id: 0ef21054-cb7e-42a5-93c5-c817f2de1847
spl set id: 06c855f9-9de2-4844-a726-73169a4724e9

Reported adverse events (FAERS/openFDA)#

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