CLEARING TONIC- salicylic acid liquid

CLEARING TONIC by

Drug Labeling and Warnings

CLEARING TONIC by is a Otc medication manufactured, distributed, or labeled by Halogent, LLC (DBA Exposed Skin Care) . Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

PURPOSE

ACNE TREATMENT

ACTIVE INGREDIENT

ACTIVE INGREDIENT

SALICYLIC ACID (1%)

WARNINGS

WARNINGS FOR EXTERNAL USE ONLY

INDICATIONS & USAGE

USE

FOR THE TREATMENT OF ACNE

ASK DOCTOR/PHARMACIST

Ask a doctor or pharmacist before use if you are using other topical acne medications at the same time or immediately following use of this product. This may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

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.

WHEN USING

When using this product avoid contact with eyes. If contact occurs, flush thoroughly with water.

DOSAGE & ADMINISTRATION

Directions

Gently apply a small amount of Clearing Tonic to affected area using your bare hands. Avoid contact with eyes.

• Cleanse the skin thoroughly before applying medication
• Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three 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.

INACTIVE INGREDIENT

Inactive Ingredients

Water, glycolic acid, propylene glycol, azelaic acid, hamamelis virginiana (witch hazel) distillate, dimethylethanolamine, phenoxyethanol, sodium hydroxide, camellia sinensis (green tea) leaf extract, passiflora edulis (passion) flower extract, aloe barbadensis leaf extract, salvia officinalis (sage) leaf extract, fragrance.

QUESTIONS

Questions? 1-866-404-7656 or www.exposedskincare.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CLEARING TONIC 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55878-104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCOLIC ACID (UNII: 0WT12SX38S)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
AZELAIC ACID (UNII: F2VW3D43YT)
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
DEANOL (UNII: 2N6K9DRA24)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)
HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6)
LICORICE (UNII: 61ZBX54883)
OCIMUM BASILICUM FLOWERING TOP (UNII: 7SAB275FP2)
CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)
PASSIFLORA EDULIS FLOWER (UNII: SY49TH8VUA)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SALVIA OFFICINALIS FLOWERING TOP (UNII: 48JCS720FN)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55878-104-54	1 in 1 BOX
1	NDC: 55878-104-24	120 mL in 1 BOTTLE
2	NDC: 55878-104-22	60 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	02/07/2013

Labeler - Halogent, LLC (DBA Exposed Skin Care) (790961697)