Label: DR JOE LAB CLARIFYING TONER- clarifying toner salicylic acid 1% liquid
- NDC Code(s): 82557-600-01, 82557-600-02
- Packager: DR JOE LAB
- Category: HUMAN OTC DRUG LABEL
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 July 20, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DR JOE LAB CLARIFYING TONER
- PURPOSE
- INDICATIONS & USAGE
-
DOSAGE & ADMINISTRATION
Apply small amount on your face or affected area
• clean the skin thoroughly before applying this product.
• cover the entire affected area with a thin layer one to three times daily.
• because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
• if bothersome dryness or peeling occurs, reduce application to once a day or every other day. - WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- INACTIVE INGREDIENT
- DESCRIPTION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DR JOE LAB CLARIFYING TONER
clarifying toner salicylic acid 1% liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82557-600 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1 g in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM HYDROXIDE (UNII: 55X04QC32I) FYTIC ACID (UNII: 7IGF0S7R8I) WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) LAVENDER OIL (UNII: ZBP1YXW0H8) BENZYL ALCOHOL (UNII: LKG8494WBH) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) OLIVE OIL (UNII: 6UYK2W1W1E) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) ALOE VERA LEAF (UNII: ZY81Z83H0X) HYALURONATE SODIUM (UNII: YSE9PPT4TH) GLYCERIN (UNII: PDC6A3C0OX) DEHYDROACETIC ACID (UNII: 2KAG279R6R) GLYCERETH-8 (UNII: EL2NFK7352) PANTHENOL (UNII: WV9CM0O67Z) PIROCTONE OLAMINE (UNII: A4V5C6R9FB) EDETATE DISODIUM (UNII: 7FLD91C86K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82557-600-01 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/01/2022 2 NDC:82557-600-02 236.59 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M006 07/01/2022 Labeler - DR JOE LAB (122311139)