SupreH Ringworm Treatment Balm

Manufacturer
Shenzhen Xinxin Yunhai Technology Co., Ltd.
Effective date
2025-08-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:10:48

Label at a glance#

ProductSupreH Ringworm Treatment Balm
Active ingredientCLOTRIMAZOLE
Label structure14 sections

Dosage and administration

wash affected area and dry thoroughly; apply a thin layer over affected area twice daily (morning and night); supervise children in the use of this product; use daily for 4 weeks; if condition persists longer, ask a doctor; this product is not effective on the scalp or nails

Storage and handling

Store between 68 to 77 F (20 to 25 C)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Clotrimazole 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Use

INDICATIONS & USAGE SECTION

cures most ringworm; relieves itching, redness, irritation and discomfort which accompany this condition

Warnings

WARNINGS SECTION

For external use only. Do not use on children under 2 years of age unless directed by a doctor.

Do not use

OTC - DO NOT USE SECTION

on children under 2 years of age unless directed by a doctor.

When Using this product

OTC - WHEN USING SECTION

avoid contact with the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation occurs; there is no improvement within 4 weeks

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

irritation occurs; there is no improvement within 4 weeks

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

wash affected area and dry thoroughly; apply a thin layer over affected area twice daily (morning and night); supervise children in the use of this product; use daily for 4 weeks; if condition persists longer, ask a doctor; this product is not effective on the scalp or nails

Other information

STORAGE AND HANDLING SECTION

Store between 68 to 77 F (20 to 25 C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Camphor (Synthetic), Gentian, Glycerin, Methylparaben, Menthol, Propylene Glycol, Dimethicone, Triethanolamine, Beeswax, Tea Tree Oil, Aloe Vera, Witch Hazel, Chamomile, Calendula

Questions or comments?

OTC - QUESTIONS SECTION

Contact us at support@soothpro.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CLOTRIMAZOLE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b64d2752-34ef-378a-1f4f-8bff32b0d1aeProduct name420250626
cb7783e0-feaa-7e56-fb3b-d43b6efa77c9Product name220250121
f31c883b-7ebf-1c60-f3b6-4ba41e8ff7a6Product name220151106
f5395dd2-4395-d8c6-3477-8c2d4a2f951cProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83818-022-01SupreH Ringworm Treatment Balm80 g in 1 JARCREAM801

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83818-02283818-022-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
SupreH Ringworm Treatment BalmSUPREH RINGWORM TREATMENT BALMShenzhen Xinxin Yunhai Technology Co., Ltd.3c77222b-d92e-84b0-e063-6294a90aadd72025-08-16WarningsExact identifier
ndc (package): 83818-022-01
ndc (product): 83818-022
ndc11 (package): 83818002201
spl id: 3c77222b-d92f-84b0-e063-6294a90aadd7
spl set id: 3c77222b-d92e-84b0-e063-6294a90aadd7

Reported adverse events (FAERS/openFDA)#

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