Label: GLOVERS MEDICATED ANTI-DANDRUFF SCALP- salicylic acid solution
- NDC Code(s): 12022-011-00
- Packager: J. Strickland & Co.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 21, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Use
-
Warnings:
For External Use Only.
When using this product
- avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Stop use and ask a doctor if
condition worsens or does not improve after regular use of this product as directed.
- Directions:
- Inactive Ingredients:
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
GLOVERS MEDICATED ANTI-DANDRUFF SCALP
salicylic acid solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:12022-011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BENZYL ALCOHOL (UNII: LKG8494WBH) MENTHOL (UNII: L7T10EIP3A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:12022-011-00 1 in 1 CARTON 11/05/2001 1 75 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 11/05/2001 Labeler - J. Strickland & Co. (007023112) Registrant - J. Strickland & Co. (007023112) Establishment Name Address ID/FEI Business Operations J. Strickland & Co. 007023112 manufacture(12022-011)