ACTIVE CLEAR FACIAL WASH- salicylic acid liquid

Active Clear Facial Wash by

Drug Labeling and Warnings

Active Clear Facial Wash by is a Otc medication manufactured, distributed, or labeled by Seacret Spa LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Salicylic Acid 2.0%

Purpose

Acne treatment

Indications

For treatment of acne

Warnings

For external use only

When using this product

• Avoid contact with the eyes. If product gets into eyes, rinse thoroughly with water.
• Using other topical acne medications at the same time or immediately following use of this product 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. If swallowed, get medical help or contact a Poison Control Center right away. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

Directions

Apply cleanser on wet facial skin, gently massaging in circular motions until a creamy lather forms. Avoid the eye area. Rinse well with lukewarm water. For best results, use twice daily.

Inactive ingredients

water/aqua, sodium cocoyl isethionate, cetearyl alcohol, stearic acid, glycerin, laureth-3, phenoxyethanol, ethylhexylglycerin, sodium hydroxide, fragrance/parfum, disodium EDTA, maris sal (dead sea mineral water), caramel, butylphenyl methylpropional, hexyl cinnamal, linalool

PRINCIPAL DISPLAY PANEL - 100 mL Tube Label

SEACRET™
MINERALS FROM THE DEAD SEA

clear

ACTIVE CLEAR
FACIAL WASH
For oily, acne-prone skin

2%
SALICYLIC
ACID

3.4 fl.oz / 100 mL

INGREDIENTS AND APPEARANCE

ACTIVE CLEAR FACIAL WASH 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69915-001
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
Water (UNII: 059QF0KO0R)
Sodium Cocoyl Isethionate (UNII: 518XTE8493)
Cetostearyl alcohol (UNII: 2DMT128M1S)
Stearic Acid (UNII: 4ELV7Z65AP)
Glycerin (UNII: PDC6A3C0OX)
Laureth-3 (UNII: F32E4CB0UJ)
Phenoxyethanol (UNII: HIE492ZZ3T)
Ethylhexylglycerin (UNII: 147D247K3P)
Sodium Hydroxide (UNII: 55X04QC32I)
Edetate Disodium (UNII: 7FLD91C86K)
Caramel (UNII: T9D99G2B1R)
Butylphenyl Methylpropional (UNII: T7540GJV69)
.Alpha.-Hexylcinnamaldehyde (UNII: 7X6O37OK2I)
Linalool, (+/-)- (UNII: D81QY6I88E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69915-001-01	100 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	06/12/2015

Labeler - Seacret Spa LLC (363790846)