WITCH HAZEL PORE CLARIFYING TONER 8 OZ- salicylic acid 2% gel

Witch Hazel Pore Clarifying Toner by

Drug Labeling and Warnings

Witch Hazel Pore Clarifying Toner by is a Otc medication manufactured, distributed, or labeled by China Ningbo Shangge Cosmetic Technology Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Purpose

Acne treatment

ACTIVE INGREDIENT

Active Ingredient

Salicylic Acid 2%

DOSAGE & ADMINISTRATION

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

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

INACTIVE INGREDIENT

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

WARNINGS

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WITCH HAZEL PORE CLARIFYING TONER  8 OZ
salicylic acid 2% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58503-121
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ALCOHOL (UNII: 3K9958V90M)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
WITCH HAZEL (UNII: 101I4J0U34)
MENTHOL (UNII: L7T10EIP3A)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58503-121-01	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/11/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	12/11/2019

Labeler - China Ningbo Shangge Cosmetic Technology Corp. (529287434)

Establishment
Name	Address	ID/FEI	Business Operations
China Ningbo Shangge Cosmetic Technology Corp.		529287434	manufacture(58503-121)