Witch Hazel Pore Clarifying Toner

Manufacturer
Ningbo Rejoice International | China Ningbo Shangge Cosmetic Technology Corp.
Effective date
2025-02-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:55:14

Label at a glance#

ProductWitch Hazel Pore Clarifying Toner 8 oz
Active ingredientSALICYLIC ACID
Label structure9 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Purpose

Acne treatment

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Salicylic Acid 2%

DOSAGE & ADMINISTRATION SECTION

Directions

  • Cleanse skin thoroughly before applying medication.
  • Cover the entire affected area with a thin layer 1 to 3 times daily using a cotton ball or pad.
  • Because excessive drying of the skin may occur, start with 1 application daily, then gradually increase to 2 or 3 times daily if needed or as directed by a doctor.
  • If bothersome dryness or peeling occurs, reduce application to once a day or every other day

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

If swallowed get medical help or contact a poison control center right away.

INACTIVE INGREDIENT SECTION

Water, alcohol denat., isopropyl alcohol, hamamelis virginiana (witch hazel) water, PEG-40 hydrogenated castor oil, glycerin, fragrance, sodium hydroxide, disodium EDTA, menthol

WARNINGS SECTION

Warnings

For external use only

Flammable: Keep away from fire or flame

When using this product

  • Skin irritation and dryness are more likely to occur if you use another topical acne medication at the same time. If irritation occurs, oinly use one topical acne medication at a time.
  • Avoid contact with eyes. If contact occurs, rinse thoroughly with water

INDICATIONS & USAGE SECTION

Uses

  • Clears up acne blemishes
  • Penetrates pores to control acne blemishes
  • Helps prevent new acne blemishes from forming

OTHER SAFETY INFORMATION

Other Information

Store at room temperature

Questions / Comments?

1-855-345-5575

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57337-104-012025-02-13C16284748780-12cef2736-5baf-d83d-e063-dadaa90ab31fWitch Hazel Pore Clarifying Toner
57337-104-012025-01-30C16284748780-12cef2736-5baf-d83d-e063-dadaa90ab31fWitch Hazel Pore Clarifying Toner

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57337-104-01Witch Hazel Pore Clarifying Toner8 oz237 mL in 1 BOTTLEGEL2372

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57337-104WITCH HAZEL PORE CLARIFYING TONER 8 OZ (SALICYLIC ACID 2%) GEL [NINGBO REJOICE INTERNATIONAL]2Current NDC, Legacy NDC, 1 package rows20250215_99748785-8321-7bbf-e053-2a95a90a16c9.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57337-10457337-104-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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
Witch Hazel Pore Clarifying Toner 8 ozSALICYLIC ACID 2%Ningbo Rejoice International99748785-8321-7bbf-e053-2a95a90a16c92025-02-13WarningsExact identifier
ndc (package): 57337-104-01
ndc (product): 57337-104
ndc11 (package): 57337010401
spl id: 2e00e61d-042b-1f00-e063-6294a90aff43
spl set id: 99748785-8321-7bbf-e053-2a95a90a16c9

Reported adverse events (FAERS/openFDA)#

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