BENZOCAINE- orajel severe toothache liquid
Church & Dwight Co., Inc.
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.
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Use for the temporary relief of pain due to • canker sores • minor injury of the mouth and gum • minor irritation of the mouth and gums caused by dentures
Warnings
Allergy Alert: do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other "caine" anesthetics
Flammable: keep away from fire or flame. Avoid smoking during application and until this product has been dried
Do not use • more than directed • for more than 7 days unless directed by a physician or healthcare provider
Stop use and ask a physician if • swelling, rash or fever develops • irritation, pain or redness persists or worsens • symptoms do not improve in 7 days • allergic reaction occurs
Keep out of reach of children.
In case of overdose or allergic reaction, get medical help or contact a Poison Control Center right away
Directions • remove imprinted safety seal from bottle cap
Adults and children 2 years of age and over
Apply product with cotton swab or finger to the affected area. Use up to 4 times a day or ad directed by a physician or healthcare provider
Children under 12 years of age
Should be supervised in the use of this product
Children under 2 years of age
Ask a physician or healthcare provider
Other Information • do not use if imprinted bottle seal is broken or missing prior to opening • do not continuously
Inactive Ingredients alcohol (54.5% by volume), flavor, polyehtylene glycol, red 40, sodium saccarin, water, yellow 5
BENZOCAINE
orajel severe toothache liquid |
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Labeler - Church & Dwight Co., Inc. (001211952) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
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Accupac | 071609663 | manufacture(10237-767) |