DANDRUFF RELIEF DAYLOGIC- salicylic acid 3.0% liquid 
Rite Aid

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.

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Drug Facts

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

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

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.

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

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

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DANDRUFF RELIEF  DAYLOGIC
salicylic acid 3.0% liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-1237
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) Salicylic Acid3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11822-1237-374 mL in 1 BOTTLE; Type 0: Not a Combination Product09/30/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H09/30/2016
Labeler - Rite Aid (014578892)
Registrant - Product Quest Mfg (927768135)
Establishment
NameAddressID/FEIBusiness Operations
Product Quest Mfg927768135manufacture(11822-1237) , label(11822-1237)

Revised: 6/2018
Document Id: 146a62ff-ed84-44f7-a94e-f44003b08d06
Set id: 8d173e79-6459-4545-84fe-d9817a309b69
Version: 1
Effective Time: 20180621
 
Rite Aid