Label: DANDRUFF RELIEF DAYLOGIC- salicylic acid 3.0% liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 11822-1237-3 - Packager: Rite Aid
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 21, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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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
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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)