SEBORRHEIC DERMATITIS AND PSORIASIS- roycederm seborrheic dermatitis and psoriasis shampoo shampoo

Seborrheic Dermatitis and Psoriasis by

Drug Labeling and Warnings

Seborrheic Dermatitis and Psoriasis by is a Otc medication manufactured, distributed, or labeled by Ehy Holdings LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

ARTEMISIA EXTRACT 【FHFI】3%

Purpose

Seborrheic

Use

Relieves and helps preventrecurrence of scalp: itching, flakingscaling, redness, and irritationassociated with psoriasis andseborrheic dermatitis.

Warnings

For external use only

Do not use

Do not use morethan 3 times daily. Children under12 years: ask a doctor

WHEN USING

When using this productavoid contact with eyes.

STOP USE

condition worsens or does notimprove after regular use asdirected

KEEP OUT OF REACH OF CHILDREN

lf swallowed, get medical help orcontact a Poison Control Center (1-800-222-1222) right away.

Directions

Adult and children over 12 vears or old. Wash handsbefore and after applying the cream. Apply to affected area at the firstsign of blisters, sores, or tingling sensation. Rub in gently andthoroughly. Do not use more than 3 times daily. Children under 12years: ask a doctor

Other information

Stor at room temperature and out of directsunlight.

Inactive ingredients

Purified water, Artemisia extractsSophora Flavescens, Cnidium Monnieri (L) Cuss., Kochiascoparia, Dictamni Cortex, Smilax Glabra Roxb, SolidagoDecurrens, Phellodendron amurense Ruprecht., GleditsiaSinensis

ASK DOCTOR

than 3 times daily. Children under12 years: ask a doctor

QUESTIONS

Visit www.roycederm.com

Package Label - Principal Display Panel

81799-007-1

1

81799-007-1

2

81799-007-1

3

INGREDIENTS AND APPEARANCE

SEBORRHEIC DERMATITIS AND PSORIASIS 
roycederm seborrheic dermatitis and psoriasis shampoo shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81799-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WORMWOOD (UNII: F84709P2XV) (WORMWOOD - UNII:F84709P2XV)	WORMWOOD	3 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)
WATER (UNII: 059QF0KO0R)
SMILAX GLABRA WHOLE (UNII: H51N91QNEB)
CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)
BASSIA SCOPARIA POLLEN (UNII: 07A108ZKW5)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81799-007-01	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/11/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/11/2023

Labeler - Ehy Holdings LLC (117322715)

Establishment
Name	Address	ID/FEI	Business Operations
Ehy Holdings LLC		117322715	manufacture(81799-007)