Warm Sap Patch

Manufacturer
E-House Korea Holdings International
Effective date
2010-01-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:23:13

Label at a glance#

ProductWarm Sap Patch
Active ingredientSTARCH, CORN
Label structure11 sections

Storage and handling

Avoid storing product in direct sunlight.  Keep it in a dry and cool place.

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BOX LABEL
BOX LABEL

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:

Topical Starch

OTC - WHEN USING SECTION

When using this product:
- Do not use other than directed
- Do not stretch the adhesive portion
- Do not remove the patch's contents
- Discard patch if ripped

OTC - DO NOT USE SECTION

Do Not Use:
- on wounds or damaged skin
- if allergic to any of this product's ingredients
- With or at the same time as other external products

OTC - STOP USE SECTION

Stop Use and Consult Medical Professional
- if allergic reaction or irritation occurs
- if pregnant, nursing or under medical treatment

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 immediately

STORAGE AND HANDLING SECTION

Avoid storing product in direct sunlight.  Keep it in a dry and cool place.

WARNINGS SECTION

For external use only

DESCRIPTION SECTION

How To Use:
Apply to arches of the feet, center of the hands, toes and fingers since many of the main bodily organs connect at these locations.  The patch may be used at any time but is usually most convenient just prior to bed.  For localized treatment, place the patch on any aching, sprained or sore area.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Chitosan, Micro Capsule, Polysaccharide, Agaricus, Mugwort Extract, Vitamin C, Loquat Extract, Tourmaline, Eucalyptus Oil

DOSAGE & ADMINISTRATION SECTION

Directions:
Adults and children over 4 years
Step 1: Clean and dry area for the patch to be attached
Step 2: Remove the protective cover sheet and gently apply
Step 3: Leave it on at least 4 hours before removal
Children under 4 years, consult your medical professional

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50387-200-142019-10-21C16284748780-1956f9ecf-c357-621f-e053-dbdaa90a74ad47df4809-90e1-4a87-a9da-b919d89bf691

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50387-200-14Warm Sap Patch4 g in 1 BOXPOULTICE41

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50387-200WARM SAP PATCH (TOPICAL STARCH) POULTICE [E-HOUSE KOREA HOLDINGS INTERNATIONAL]1Legacy NDC, 1 package rows20100115_47df4809-90e1-4a87-a9da-b919d89bf691.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
STARCH, CORNACTIVE INGREDIENTO8232NY3SJ1
STARCH, CORNACTIVE MOIETYO8232NY3SJ1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50387-20050387-200-14

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
STARCH, CORNO8232NY3SJACTIB

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
cd5cff0a-ecaa-42a5-8a50-a1fafbf610a647df4809-90e1-4a87-a9da-b919d89bf6912010-01-11WarningsExact identifier
spl id: cd5cff0a-ecaa-42a5-8a50-a1fafbf610a6
spl set id: 47df4809-90e1-4a87-a9da-b919d89bf691

Reported adverse events (FAERS/openFDA)#

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