Label: DYNAREX GREEN- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 67777-307-01, 67777-307-02 - Packager: Dynarex Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 October 22, 2014
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- WARNINGS
- DO NOT USE
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- KEEP OUT OF REACH OF CHILDREN
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DYNAREX GREEN
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67777-307 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.3 mL in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) LAVENDER OIL (UNII: ZBP1YXW0H8) OLEIC ACID (UNII: 2UMI9U37CP) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) ROSIN (UNII: 88S87KL877) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67777-307-01 473 mL in 1 BOTTLE 2 NDC:67777-307-02 3785 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/28/2014 Labeler - Dynarex Corporation (008124539) Registrant - Dynarex Corporation (008124539)
