Antibacterial by Continental Manufacturing Chemist, Inc.
Dosage form: gel Ingredients: ALCOHOL 620g in 1.0kg Labeler: Continental Manufacturing Chemist, Inc. NDC Code: 49794-009
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.
Ethyl Alcohol 62%
To decrease bacteria on skin
For external use only
Flammable! Keep away from fire or flame. Do not use in eye; if this happens rinse thoroughly with water.
Do not use
Ask a doctor before use if
Ask a doctor or pharmacist before use if
When using this product
Stop use and ask a doctor if
irritation or redness develops and persists more than 72 hours
Keep out of reach of children
If ingested get medical help or contact a Poison Control Center right away
Wet hands thoroughly with product and allow to dry without wiping. Children under six should be supervised while using this product.
Do not store above 105F (40C)
Amino Methyl Propanol, Carbomer, FD&C Blue #1, Fragrance, Propylene Glycol, Purified Water
Principal Display Panel
Antibacterial Gel Labels
HUMAN OTC DRUG
Item Code (Source)
Route of Administration
Active Ingredient/Active Moiety
Basis of Strength
620 g in 1.0 kg
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)
FD&C BLUE NO. 1
1000 kg in 1 CONTAINER
Application Number or Monograph Citation
Marketing Start Date
Marketing End Date
OTC MONOGRAPH NOT FINAL
Labeler - Continental Manufacturing Chemist, Inc.
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