Label: SEBORRHEIC DERMATITIS AND PSORIASIS CREAM- roycederm seborrheic dermatitis and psoriasis cream cream
- NDC Code(s): 81799-006-01
- Packager: Ehy Holdings LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated January 12, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- ASK DOCTOR
- QUESTIONS
- Package Label - Principal Display Panel
-
INGREDIENTS AND APPEARANCE
SEBORRHEIC DERMATITIS AND PSORIASIS CREAM
roycederm seborrheic dermatitis and psoriasis cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81799-006 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) BORNEOL (UNII: M89NIB437X) 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:81799-006-01 100 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(81799-006)