Orajel for Cold Sores description, usages, side effects, indications, overdosage, supplying and lots more!

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Orajel for Cold Sores

Church & Dwight Co., Inc.

DRUG FACTS




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients          Purpose
Benzocaine 20%                  Oral pain reliever

White petrolatum 74.44%      Skin protectant

Purpose

Uses  temporarily relieves pain and dryness; softens crusts (scabs) associated with cold sores, fever blisters


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

Do not use
more than is directed
for more than 7 days unless told to do so by a dentist or doctor

Stop use and ask a doctor if
condition worsens
symptoms do not improve in 7 days
symptoms clear up and occur again within a few days

Keep out of reach of children
In case of overdose, get medical help or contact a Poison Control Center right away

Directions    cut open tip of tube on score mark; do not use if tube tip is cut prior to opening

Adults and children 2 years of age and over          Apply to affected area not more than 3 to 4                                                                            times daily
                                                                          
Children under 12 years of age                             Should be supervised in the use of this                                                                               product

Children under 2 years of age                               Ask a doctor

Inactive ingredients

cholecalciferol, methylparaben, mineral oil, propylene glycol, propylparaben, prunella vulgaris leaf extract, retinyl palmitate (vitamin A palmitate), tocopherol, tocopheryl acetate (vitamin E acetate), water, zea mays (corn) oil

Questions or comments?  call us at 1-800-952-5080 M-F 9am-5pm or visit our website at www.orajel.com

Orajel for Cold Sores

Orajel for Cold Sores

Benzocaine CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10237-750
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BENZOCAINE Benzocaine 200 mg
petrolatum 744.4 mg

Inactive Ingredients

Ingredient Name Strength
CHOLECALCIFEROL
METHYLPARABEN
Mineral Oil
polyethylene glycol
PRUNELLA VULGARIS
VITAMIN A PALMITATE
ALPHA-TOCOPHEROL
.ALPHA.-TOCOPHEROL ACETATE, D-
water
CORN OIL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 5.9 in 1 TUBE
2 NDC:10237-750-21 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part356 2010-07-27


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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