Label: ACTIOGEN ACNE DOTS TREATMENT- acne treatment patch
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Contains inactivated NDC Code(s)
NDC Code(s): 69186-001-10 - Packager: Actiogen Corp
- 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 14, 2015
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Use
- DOSAGE & ADMINISTRATION
- Warnings
- When Using This Product
- Stop Using This Product
- Do Not Use
- Consult a physician
- Keep Out of Reach of Children
- Other Information
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ACTIOGEN ACNE DOTS TREATMENT
acne treatment patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69186-001 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 mg in 100 mg Inactive Ingredients Ingredient Name Strength ACRYLIC ACID (UNII: J94PBK7X8S) 96 mg in 100 mg PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 1 mg in 100 mg ZINC OXIDE (UNII: SOI2LOH54Z) 1 mg in 100 mg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69186-001-10 10 in 1 BOX 08/01/2014 1 2 mg in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 08/01/2014 Labeler - Actiogen Corp (967358057)