CLEAR PORE SERUM- salicylic acid gel

CLEAR PORE SERUM by

Drug Labeling and Warnings

CLEAR PORE SERUM 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 (1.0%)

INDICATIONS & USAGE

USE

FOR THE TREATMENT OF ACNE

WARNINGS

WARNINGS FOR EXTERNAL USE ONLY

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

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 serum 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, hamamelis virginiana (witch hazel) distillate, glycerin, propylene glycol, peg 120 methyl glucose dioleate, polyquaternium-37, hydrogenated polydecene, tricedeth-6, spiraea ulmaria (meadowsweet) extract, glycyrrhiza glabra (licorice) root extract, ocimum basilicum extract , camellia sinensis (green tea) leaf extract, panthenol, phenoxyethanol, fragrance.

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.

QUESTIONS

Questions? 1-866-404-7656

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CLEAR PORE SERUM 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55878-103
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)
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
POLYQUATERNIUM-37 (10000 MPA.S) (UNII: 41QWS48DFN)
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)
PANTHENOL (UNII: WV9CM0O67Z)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55878-103-52	1 in 1 BOX
1	NDC: 55878-103-12	50 mL in 1 TUBE
2	NDC: 55878-103-11	26 mL in 1 TUBE

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)