NUPHARMISTO PSORIASIS ECZEMA CREAM- psoriasis eczema cream cream

Nupharmisto Psoriasis Eczema Cream by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

RHINACANTHUS NASUTUS 7%
DICTAMNUS DASYCARPUS TURCZ 7%
VIOLA PHILIPPICA 3%
EUPHORBIA HIRTA 2%
MURRAYA EXOTICA 2%
SOPHORA FLAVESCENS ALT 1.8%
MENTHA HAPLOCALYX BRIQ 1.2%

Purpose

Relieve the itching, dry and scaling

Use

Temporarily protects and helps relieveminor skin irritation and itching due to: PsoriasisEczema, Seborrheic Dermatitis, Molluscum,Shingles, Severe Boils, Fungal lnfections, Warts.Other Resistant Skin Conditions

Warnings

For external use only.

WHEN USING SECTION

Avoid contact with eyeslf contact occurs, rinse the eyes thoroughly with water

STOP USE section

Condition worsens ordoes not improve after regular use as directed

KEEP OUT OF REACH OF CHILDREN

If swallowed, getmedical help or contact aPoison Control Center(1-800-222-1222) right away.

ASK DOCTOR

Apply a thin layer over the affected areatwice daily(morning and night), or asdirected by a doctor.
If the condition persists longer, consult a doctor.

Directions

Apply a small amount to theproblem areas with circularmotions for 3 minutes till theskin absorbs the cream.

Other information

Store at 59-86ff(15-30°CClose the cap tightly after use.

Inactive ingredients

Smilax Glabra, Sophora Flavescens, CnidiumMonnier(L) Cuss, Fructus Kochiae, Pseudolarixamabillis, Cortex Dictamni, Stemonatuberosalour, Mentha, Glycyrrhetinic Acid

PACKAGE LABEL - PRINCIPAL DISPLAY PANEL

81799-010-01

INGREDIENTS AND APPEARANCE

NUPHARMISTO PSORIASIS ECZEMA CREAM 
psoriasis eczema cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81799-010
Route of Administration	EXTRACORPOREAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHA CANADENSIS TOP (UNII: 610T51U707) (MENTHA CANADENSIS TOP - UNII:610T51U707)	MENTHA CANADENSIS TOP	1.2 mg  in 100 mL
VIOLA PHILIPPICA WHOLE (UNII: O176VC3N54) (VIOLA PHILIPPICA WHOLE - UNII:O176VC3N54)	VIOLA PHILIPPICA WHOLE	3 mg  in 100 mL
SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L) (SOPHORA FLAVESCENS WHOLE - UNII:X8KX602M5L)	SOPHORA FLAVESCENS WHOLE	1.8 mg  in 100 mL
RHINACANTHUS NASUTUS LEAF (UNII: 97OQD55S9I) (RHINACANTHUS NASUTUS LEAF - UNII:97OQD55S9I)	RHINACANTHUS NASUTUS LEAF	7 mg  in 100 mL
DICTAMNUS DASYCARPUS WHOLE (UNII: IM7ZCU30YH) (DICTAMNUS DASYCARPUS WHOLE - UNII:IM7ZCU30YH)	DICTAMNUS DASYCARPUS WHOLE	7 mg  in 100 mL
EUPHORBIA HIRTA (UNII: L13YF113GN) (EUPHORBIA HIRTA - UNII:L13YF113GN)	EUPHORBIA HIRTA	2 mg  in 100 mL
MURRAYA PANICULATA FRUIT (UNII: PE014Z7R7C) (MURRAYA PANICULATA FRUIT - UNII:PE014Z7R7C)	MURRAYA PANICULATA FRUIT	2 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BORNEOL (UNII: M89NIB437X)
SMILAX GLABRA WHOLE (UNII: H51N91QNEB)
CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)
SCOPARIA DULCIS LEAF (UNII: 1PD9Z8123P)
SOLIDAGO DECURRENS WHOLE (UNII: Y026RJV99T)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81799-010-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	M032	03/15/2023

Labeler - Ehy Holdings LLC (117322715)

Establishment
Name	Address	ID/FEI	Business Operations
Ehy Holdings LLC		117322715	manufacture(81799-010)