HEMORRHOID, FISSURE, PROCTALGIA RELIEF WASH- carbon, panthenol, sodium hyaluronate liquid

Hemorrhoid, Fissure, Proctalgia Relief Wash by

Drug Labeling and Warnings

Hemorrhoid, Fissure, Proctalgia Relief Wash by is a Otc medication manufactured, distributed, or labeled by WU XI ZHONG ZHI WEI NA TECHNOLOGY CO., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Carbon 0.1%
Panthenol 0.2%
Sodium Hyaluronate 0.05%
Glycerin 2%

PURPOSE

Adsorbent and detoxifying
Healing and barrier protection
Hydration and wound healing
Humectant and moisturizing

KEEP OUT OF REACH OF CHILDREN

If swallowed, seek medicalhelp or contact a PoisonControl Center right away.

INDICATIONS & USAGE

instantly helps relieveanorectal itching and discom-fort such as pain, soreness, orburning commonly associatedwith hemorrhoids
temporarily protects theinflamed, irritated anorectalarea to make future bowelmovements less painful fromirritation and abrasion

WARNINGS

For external use.

DOSAGE & ADMINISTRATION

adults and children 12 yearsof age and over: apply to theaffected area then wash awaywith water and rinse thor-oughly 1-2 times dally orsimply while showering.For intrarectal use: applyaround the affected anal areaand then wash away withwater and rinse thoroughly.
children under 12 years ofage: ask a doctor

STORAGE AND HANDLING

STAY FRESH,COMFORTABLE,AND CLEAN.

INACTIVE INGREDIENT

Cactus Extract
Oat Bran Extract
Ophiopogon Japonicus Root Extract
Paeonia Lactiflora Root Extract
Scutellaria Baicalensis Root Extract
Water
Sodium Chloride
DMDM Hydantoin
Disodium EDTA
Polyglyceryl-10 Laurate
Sodium Sulfate
Butylene Glycol
Phenoxyethanol
Lauryl Alcohol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HEMORRHOID, FISSURE, PROCTALGIA RELIEF WASH 
carbon, panthenol, sodium hyaluronate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84533-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	2 g  in 100 mL
HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY)	HYALURONATE SODIUM	0.05 g  in 100 mL
PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z)	PANTHENOL	0.2 g  in 100 mL
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10)	ACTIVATED CHARCOAL	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
DMDM HYDANTOIN (UNII: BYR0546TOW)
PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
LAURYL ALCOHOL (UNII: 178A96NLP2)
POLYGLYCERYL-10 LAURATE (UNII: MPJ2Q8WI8G)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
OAT BRAN (UNII: KQX236OK4U)
OPUNTIA FICUS-INDICA (UNII: 23Z87HTQ6P)
SODIUM SULFATE (UNII: 0YPR65R21J)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
OPHIOPOGON JAPONICUS ROOT (UNII: 90PS6JV9GZ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84533-002-01	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/26/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	07/26/2024

Labeler - WU XI ZHONG ZHI WEI NA TECHNOLOGY CO., Ltd. (412779339)

Establishment
Name	Address	ID/FEI	Business Operations
WU XI ZHONG ZHI WEI NA TECHNOLOGY CO., Ltd.		412779339	manufacture(84533-002)