- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
-
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
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DANDRUFF RELIEF DAYLOGIC
salicylic acid 3.0% liquidProduct 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)