DANDRUFF RELIEF DAYLOGIC- salicylic acid 3.0% liquid

Dandruff Relief by

Drug Labeling and Warnings

Dandruff Relief by is a Otc medication manufactured, distributed, or labeled by Rite Aid, Product Quest Mfg. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                                    Purpose
Salicylic Acid 3%.................................... Psoriasis, Anti-dandruff,
                                                              and Seborrheic dermatitis

PURPOSE

INDICATIONS & USAGE

Uses
Relieves and controls the following symptoms associated with
dandruff, seborrheic dermatitis and psoriasis
scalp itching flaking irritation redness scaling

WARNINGS

Warnings
For external use only
Flammable - store away from fire or flame.
Allergy alert: do not use if allergic to salicylates or aspirin.
Consult a doctor before use
if condition covers a large area of the body.
Stop use and consult a doctor
if condition worsens or does not improve with regular use of
this product as directed.
When using this product
avoid contact with eyes. If contact occurs, rinse eyes
thoroughly with water.
Keep out of the reach of children. If swallowed get medical
help or contact a Poison Control Center right away. If pregnant
or breast-feeding consult a health care professional before use.

KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION

Directions
Apply to affected areas 1 to 4 times daily or as directed by a doctor.

INACTIVE INGREDIENT

Inactive ingredients
Aloe Barbadensis Leaf Extract, Melaleuca Alternifolia (Tea Tree)
Leaf Oil, Menthol, Propylene Glycol, SD Alcohol 40-B,
Tocopheryl Acetate, Water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DANDRUFF RELIEF  DAYLOGIC
salicylic acid 3.0% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-1237
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 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TEA TREE OIL (UNII: VIF565UC2G)
Menthol (UNII: L7T10EIP3A)
Propylene Glycol (UNII: 6DC9Q167V3)
ALCOHOL (UNII: 3K9958V90M)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-1237-3	74 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/30/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	09/30/2016

Labeler - Rite Aid (014578892)

Registrant - Product Quest Mfg (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg		927768135	manufacture(11822-1237) , label(11822-1237)