RoyceDerm Sulfur Soap. by Shenzhen Situya Trading Co., Ltd. 82739-023 Complete

RoyceDerm Sulfur Soap. by

Drug Labeling and Warnings

RoyceDerm Sulfur Soap. by is a Otc medication manufactured, distributed, or labeled by Shenzhen Situya Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ROYCEDERM SULFUR SOAP.- sulfur soap soap 
Shenzhen Situya Trading Co., Ltd.

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82739-023 Complete

Active Ingredient

Sulfur 10%

Purpose

Acne Treatment

Use

for the treatment of acne.

Warnings

For external use only.

Do not use

Use caution when combining with other topical acne medications to prevent skin irritation and dryness.

When Using

When using this product avoid contact with eyes.
If contact occurs, rinse the eyes thoroughly with water.

Stop Use

stop use and ask a doctor if condition worsens or does not improve after regular use as directed.

Ask Doctor

Discontinue use and consult a doctor ifexcessive skin irritation occurs.

Keep Oot Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Create a rich lather with the mesh bag, gently apply to affected areas, leaving it on the skin for 3 to 5 minutes. Rinse thoroughly with water and pat dry with a clean towel. Incorporate into your routine 1 to 3 times a day, or as directed by a doctor, for optimal results.

Other information

■ Store at room temperature and keep away from direct sunlight.

Inactive ingredients

Water, Olea Europaea Fruit Oil, 0.25% Salicylic Acid, Lauric Acid, Stearic Acid, Sorbitol,Glycerin, Cocos Nucifera Oil, Elaeis Guineensis Oil, Botanical Acaricide, Potassium Cocoate, Lanolin, Sophora Japonica Extract, Aloe Extract, Sulfur Spring Extract, Ginseng, Coleus Forskohlii Root Oil, Tea Tree Essential Oil.

PRINCIPAL DISPLAY PANEL

ROYCEDERM SULFUR SOAP. 
sulfur soap soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82739-023
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ)
SORBITOL (UNII: 506T60A25R)
COCONUT OIL (UNII: Q9L0O73W7L)
LANOLIN (UNII: 7EV65EAW6H)
ALOE (UNII: V5VD430YW9)
TEA TREE OIL (UNII: VIF565UC2G)
4-METHYL-5-THIAZOLEETHANOL (UNII: 3XYV4I47I8)
OLIVE OIL (UNII: 6UYK2W1W1E)
COLEUS FORSKOHLII ROOT OIL (UNII: 5NXR7DJ9WO)
WATER (UNII: 059QF0KO0R)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
PALM OIL (UNII: 5QUO05548Z)
CAMPHECHLOR (UNII: 9924JQ4D5J)
STYPHNOLOBIUM JAPONICUM ROOT (UNII: LAH7966318)
STEARIC ACID (UNII: 4ELV7Z65AP)
LAURIC ACID (UNII: 1160N9NU9U)
GLYCERIN (UNII: PDC6A3C0OX)
ASIAN GINSENG (UNII: CUQ3A77YXI)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82739-023-01	232 g in 1 BOX; Type 0: Not a Combination Product	09/02/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	09/02/2024	07/22/2025

Labeler - Shenzhen Situya Trading Co., Ltd. (706154255)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Situya Trading Co., Ltd.		706154255	manufacture(82739-023) , label(82739-023)

Revised: 7/2025

Document Id: 3a8407d0-4d33-8d93-e063-6294a90a0be4

34390-5

Set id: 211a5f2c-3dfb-d735-e063-6394a90ad22c

Version: 2

Effective Time: 20250722