Label: SCARLET OIL solution
- NDC Code(s): 50989-174-26, 50989-174-29
- Packager: Vedco, Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 10, 2022
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- Official Label (Printer Friendly)
- PURPOSE
- ACTIVE INGREDIENT:
- INACTIVE INGREDIENTS:
- STORAGE AND HANDLING
-
CAUTION:
In case of deep, or puncture wounds or serious burns or if redness, irritation, or swelling persists or increases, consult a veterinarian. Keep away from eyes or mucous membranes. Avoid inhaling. A combustible liquid, do not use near open flame.
WARNING! FLAMMABLE! KEEP AWAY FROM HEAT AND OPEN FLAME. - FOOD SAFETY WARNING
- INDICATIONS:
- DIRECTIONS:
- NET CONTENTS:
- INFORMATION FOR OWNERS/CAREGIVERS
- 1PINT (16 FL OZ ) 473 mL
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INGREDIENTS AND APPEARANCE
SCARLET OIL
scarlet oil solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:50989-174 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 2.5 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50989-174-26 12 in 1 CASE 1 473 mL in 1 BOTTLE 2 NDC:50989-174-29 4 in 1 CASE 2 3785 mL in 1 JUG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/13/2016 Labeler - Vedco, Inc. (021634266) Establishment Name Address ID/FEI Business Operations FIRST PRIORITY INCORPORATED 179925722 manufacture, label