Label: EVERY MAN JACK CHARCOAL FACE SCRUB- salicylic acid cream
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Contains inactivated NDC Code(s)
NDC Code(s): 57934-5012-4 - Packager: EVERY MAN JACK
- 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 December 17, 2021
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- ACTIVE INGREDIENT
- PURPOSE
- USE
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WARNINGS
FOR EXTERNAL USE ONLY.
ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE USING OTHER TOPICAL ACNE MEDICATIONS AT THE SAME TIME OR IMMEDIATELY FOLLOWING THE USE OF THIS PRODUCT. THIS MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE MEDICATION SHOULD BE USED UNLESS DIRECTED BY A DOCTOR.
WHEN USING THIS PRODUCT: AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- INACTIVE INGREDIENTS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EVERY MAN JACK CHARCOAL FACE SCRUB
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57934-5012 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 WATER (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) HYDROGENATED JOJOBA OIL (UNII: 7F674YQ5SO) GLYCERIN (UNII: PDC6A3C0OX) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) FERROSOFERRIC OXIDE (UNII: XM0M87F357) PISTACIA LENTISCUS RESIN (UNII: 7446H202QW) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57934-5012-4 125 mL in 1 TUBE; Type 0: Not a Combination Product 06/16/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 06/16/2019 Labeler - EVERY MAN JACK (013586921) Establishment Name Address ID/FEI Business Operations DIVERSIFIED MANUFACTURING CORP 185073996 manufacture(57934-5012)