DRY SKIN RELIEF BAR- salicylic acid soap

Dry Skin Relief Bar by

Drug Labeling and Warnings

Dry Skin Relief Bar by is a Otc medication manufactured, distributed, or labeled by CP Skin Health Group, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Salicylic acid 3%

Purpose

Psoriasis and seborrheic dermatitis treatment

Uses

controls and fights the recurrence of skin itching, redness, flaking and irritation associated with psoriasis and seborrheic dermatitis

Warnings

For external use only.

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

Stop use and ask a doctor if condition worsens or does not improve after regular use of this product.

Ask a doctor if the condition covers a large area of the body.

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Directions

• use on affected areas in place of your regular soap
• for best results use at least twice a week or as directed by a physician

Other information

• store at room temperature

Inactive ingredients

Glycerin, Sodium Cocoate, Sodium Palm Kernelate, Sodium Castorate, Water, Sodium Safflowerate, Sorbitan Oleate, Sorbitol, Glycine Soja (Soybean) Protein, Evernia Prunastri (Oakmoss) Extract, Foeniculum Vulgare (Fennel) Oil, Lavandula Angustifolia (Lavender) Oil, Hamamelis Virginiana (Witch Hazel) Water, Lecithin, Aloe Barbadensis Leaf Juice Powder, Honey, Cucurbita Pepo (Pumpkin) Seed Oil, Phenylethyl Resorcinol, Camellia Sinensis (Black Tea) Leaf Extract, Tocopherol, Alcohol, Glycine Soja (Soybean) Oil.

Questions?

Please call 877.722.7546

PRINCIPAL DISPLAY PANEL - 90 g Jar Box

PCA skin®

dry skin relief bar

salicylic acid psoriasis and
seborrheic dermatitis cleanser

01 | cleanse

3.2 oz (90 g)

INGREDIENTS AND APPEARANCE

DRY SKIN RELIEF BAR 
salicylic acid soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68726-800
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM COCOATE (UNII: R1TQH25F4I)
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
SODIUM CASTORATE (UNII: 6PAR8M5DCK)
WATER (UNII: 059QF0KO0R)
SODIUM SAFFLOWERATE (UNII: UHG9F87J7K)
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
SORBITOL (UNII: 506T60A25R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
FENNEL OIL (UNII: 59AAO5F6HT)
SOYBEAN LECITHIN (UNII: 1DI56QDM62)
LAVENDER OIL (UNII: ZBP1YXW0H8)
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TEA LEAF (UNII: GH42T47V24)
PUMPKIN SEED OIL (UNII: 6E5QR5USSP)
HONEY (UNII: Y9H1V576FH)
PHENYLETHYL RESORCINOL (UNII: G37UFG162O)
SOY PROTEIN (UNII: R44IWB3RN5)
ALCOHOL (UNII: 3K9958V90M)
TOCOPHEROL (UNII: R0ZB2556P8)
EVERNIA PRUNASTRI (UNII: O3034Q5AHK)
SOYBEAN OIL (UNII: 241ATL177A)

Product Characteristics
Color	BROWN (Dark Amber Brown)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68726-800-01	1 in 1 BOX	02/22/2016
1		90 g in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph drug	M032	02/22/2016

Labeler - CP Skin Health Group, Inc. (611921669)