FDA.reportPublic FDA data

Hazel Perineal Healing Foam

Manufacturer
SHANGHAI SENWO INDUSTRY CO., LTD.
Effective date
2024-07-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:14:44

Label at a glance#

ProductHazel Perineal Healing Foam
Active ingredientWITCH HAZEL
Label structure9 sections

Storage and handling

Other informationm Store at room temperature Single use per wipe

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Witch Hazel 50%

OTC - PURPOSE SECTION

Astringent

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS & USAGE SECTION

Helps relieve pain and swelling from hemorrhoids and childbirth.

WARNINGS SECTION

For external use only

DOSAGE & ADMINISTRATION SECTION

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 SECTION

Other informationm Store at room temperature Single use per wipe

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabel2label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2166922witch hazel 50 % Topical FoamPSN1
2166922witch hazel 500 MG/ML Topical FoamSCD1
2166922witch hazel 50 % Topical FoamSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84506-001-012025-07-29C16284748780-13b156c62-2a50-fb37-e063-e6dba90a4e07Hazel Perineal Healing Foam
84506-001-022025-07-29C16284748780-13b156c62-2a50-fb37-e063-e6dba90a4e07Hazel Perineal Healing Foam

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84506-001-01Hazel Perineal Healing Foam100 mL in 1 BOTTLELIQUID1001
84506-001-02Hazel Perineal Healing Foam150 mL in 1 BOTTLELIQUID1501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84506-001HAZEL PERINEAL HEALING FOAM (WITCH HAZEL) LIQUID [SHANGHAI SENWO INDUSTRY CO., LTD.]12 package rows20240705_1c668964-2dec-a294-e063-6294a90ad3d9.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84506-00184506-001-01, 84506-001-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
TARAXACUM OFFICINALE39981FM375IACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
WATER059QF0KO0RIACT
SODIUM LAUROYL GLUTAMATENCX1UU2D33IACT
ERYTHRITOLRA96B954X6IACT
ALCOHOL3K9958V90MIACT
STEPHANIA TETRANDRA WHOLE7S7TV2F4XCIACT
WITCH HAZEL101I4J0U34ACTIB
SODIUM LAUROYL SARCOSINATE632GS99618IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
PEPPERMINT OILAV092KU4JHIACT
PHENOXYETHANOLHIE492ZZ3TIACT
TOCOPHEROLR0ZB2556P8IACT
SAURURUS CHINENSIS WHOLE6DRV3D37XSIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1c668964-2ded-a294-e063-6294a90ad3d91c668964-2dec-a294-e063-6294a90ad3d92024-07-04WarningsExact identifier
spl id: 1c668964-2ded-a294-e063-6294a90ad3d9
spl set id: 1c668964-2dec-a294-e063-6294a90ad3d9

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.