Label: DR. JOE LAB ACNE CONTROL CLARIFYING CLEANSER DR JOE LAB- acne control clarifying cleanser liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 82557-200-01 - Packager: DR JOE LAB Inc.
- 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 June 16, 2022
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- Active Ingredients
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask doctor if
- Keep out of reach of the children
- Directions
- Other information
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Inactive Ingredients
Di-anodized Water, Disodium EDTA,Caprylyl/Capryl Glucoside,Aloe vera leaf juice,Vegetable Glycerin,Lauryl Glucoside,Citric acid,
Propylene glycol,Sodium Cocoyl Isethionate, Sodium hyaluronate 1 million DA,DI-Panthenol - Vitamin B5,Acrylates/Palmeth-25 Acrylates Copolymer,Coco Glucoside,Piroctone olamine,Cocamidopropyl Hydroxysultaine,Polysorbate 20,Lavender essential oil,
Olive Oil Glycereth-8 Esters, Vitamin E Acetate,Cocamidopropylamine Oxide, Jojoba Oil, Red Raspberry seed oil, Pomegranate seed oil, Azelaic acid, Dehydroacetic Acid, Benzyl Alcohol,
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- Description
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- how to use
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR. JOE LAB ACNE CONTROL CLARIFYING CLEANSER DR JOE LAB
acne control clarifying cleanser liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82557-200 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 mL Inactive Ingredients Ingredient Name Strength HYALURONATE SODIUM (UNII: YSE9PPT4TH) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ACRYLIC ACID (UNII: J94PBK7X8S) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) LAVENDER OIL (UNII: ZBP1YXW0H8) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PANTHENOL (UNII: WV9CM0O67Z) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) COCO GLUCOSIDE (UNII: ICS790225B) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) JOJOBA OIL (UNII: 724GKU717M) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PIROCTONE OLAMINE (UNII: A4V5C6R9FB) RASPBERRY SEED OIL (UNII: 9S8867952A) DEHYDROACETIC ACID (UNII: 2KAG279R6R) ALOE VERA LEAF (UNII: ZY81Z83H0X) POLYSORBATE 20 (UNII: 7T1F30V5YH) OLIVE OIL GLYCERETH-8 ESTERS (UNII: 322K2STO13) POMEGRANATE SEED OIL (UNII: 0UI45XV0T6) AZELAIC ACID (UNII: F2VW3D43YT) BENZYL ALCOHOL (UNII: LKG8494WBH) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82557-200-01 118 mL in 1 TUBE; Type 0: Not a Combination Product 04/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M006 04/01/2022 Labeler - DR JOE LAB Inc. (122311139)