Label: ETHYL ALCOHOL- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 68345-652-17 - Packager: PSS World Medical, Inc.
- 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 April 21, 2010
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- PRINCIPAL DISPLAY PANEL
- INDICATIONS & USAGE
- INACTIVE INGREDIENT
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WARNINGS
Warnings
Flammable. Keep away from fire or flame.For external use only
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash appears and lasts
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away - ACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ETHYL ALCOHOL
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68345-652 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.62 mL in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68345-652-17 503 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333 04/21/2010 Labeler - PSS World Medical, Inc. (101822682)