HAZEL PERINEAL HEALING FOAM- witch hazel liquid

Hazel Perineal Healing Foam by

Drug Labeling and Warnings

Hazel Perineal Healing Foam by is a Otc medication manufactured, distributed, or labeled by SHANGHAI SENWO INDUSTRY CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Witch Hazel 50%

PURPOSE

Astringent

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children lfswallowed,get medica help or contact aPoison Control Center right away.

INDICATIONS & USAGE

Helps relieve pain and swelling from hemorrhoids and childbirth.

WARNINGS

For external use only

DOSAGE & ADMINISTRATION

When using this product m Avoid contact with eyes.lf contact occurs.rinsethoroughly with water..Do not exceed the recommended daily dosage unlessdirected by a doctor m Do not put this product into the rectum by using fingeror any mechanical device or applicator.

STORAGE AND HANDLING

Other informationm Store at room temperature Single use per wipe

INACTIVE INGREDIENT

Water
C12-18 ALKYL GLUCOSIDE
SODIUM LAUROYL SARCOSINATE
SODIUM LAUROYL GLUTAMATE
COCAMIDOPROPYL BETAINE
ERYTHRITOL
BUTYLENE GLYCOL
ALCOHOL
HYDROXYACETOPHENONE
1,2-HEXANEDIOL
PHENOXYETHANOL
TOCOPHEROL
SAURURUS CHINENSIS LEAF/ROOT
EXTRACT
TARAXACUM OFFICINALE
(DANDELION) LEAF EXTRACT
STEPHANIA TETRANDRA EXTRACT
MENTHA HAPLOCALYX OIL
CITRIC ACID
PEG-40 HYDROGENATED CASTOR OIL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAZEL PERINEAL HEALING FOAM 
witch hazel liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84506-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	50 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
TARAXACUM OFFICINALE (UNII: 39981FM375)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
WATER (UNII: 059QF0KO0R)
SODIUM LAUROYL GLUTAMATE (UNII: NCX1UU2D33)
ERYTHRITOL (UNII: RA96B954X6)
ALCOHOL (UNII: 3K9958V90M)
STEPHANIA TETRANDRA WHOLE (UNII: 7S7TV2F4XC)
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PEPPERMINT OIL (UNII: AV092KU4JH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TOCOPHEROL (UNII: R0ZB2556P8)
SAURURUS CHINENSIS WHOLE (UNII: 6DRV3D37XS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84506-001-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/04/2024
2	NDC: 84506-001-02	150 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/04/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	07/04/2024

Labeler - SHANGHAI SENWO INDUSTRY CO., LTD. (421273994)

Establishment
Name	Address	ID/FEI	Business Operations
SHANGHAI SENWO INDUSTRY CO., LTD.		421273994	manufacture(84506-001)