Label: CVS SCALP RELIEF- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 59779-818-12 - Packager: CVS Pharmacy
- 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 May 21, 2014
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- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor
- Keep Out of Reach of Children.
- Directions
- Other Information
- Inactive Ingredients
- Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895© 2014 CVS/pharmacyCVS.com® 1-800-SHOP CVSMade in IsraelV-XXXXX0H818 17 C1 CVS® Quality Money Back Guarantee
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Package/Label Principal Display Panel - Carton Label
CVS pharmacy™
scalp relief
Controls dandruff
Relieves and helps prevent scalp itching, irritation, redness and flaking
Infused with aloe and vitamin E
3% Salicylic acid
Psoriasis and seborrheic dermatitis treatment
Compare to the active ingredient in Scalpicin® 2 in 1 Anti-Dandruff Liquid*
2.5 FL OZ (74 mL)
*This product is not manufactured or distributed by Reckitt Benc LLC, owner of the registered trademark Scalpicin®.
CVS/pharmacy™ Scalp Relief stops the intense scalp itch associated with psoriasis and seborrheic dermatitis. Its fragrance free and non-greasy formula can be used every day to protect the scalp from irritation caused by dandruff.
Carton Label
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INGREDIENTS AND APPEARANCE
CVS SCALP RELIEF
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-818 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 WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TEA TREE OIL (UNII: VIF565UC2G) MENTHOL (UNII: L7T10EIP3A) ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) EDETATE DISODIUM (UNII: 7FLD91C86K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-818-12 1 in 1 CARTON 1 74 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 06/01/2014 Labeler - CVS Pharmacy (062312574) Establishment Name Address ID/FEI Business Operations Emilia Cosmetics Ltd 600076624 MANUFACTURE(59779-818)