Orajel Instant Relief for Teething Pain description, usages, side effects, indications, overdosage, supplying and lots more!

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Orajel Instant Relief for Teething Pain

Church & Dwight Co., Inc.

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients

               

Purpose

Purpose

Uses

USE

Warnings
Allergy Alert:




Do not use
  • more than directed
  • for more than 7 days unless directed by a physician or healthcare provider
When using this produ ct

Stop use and ask a doctor if
  • sore mouth symptoms do not improve in 7 days,
  • irritation, pain or redness does not go away,
  • swelling, rash or fever develops

Keep out of reach of children.
Directions
  • wash hands
  • cut open tip of tube on score mark
  • use your fingertip or cotton applicator to apply a small pea-size amount of Orajel and spread over the gums
  • apply to the affected area up to 4 times daily or as directed by a physician or healthcare provider
  • for children under 2 years of age, consult a physician or healthcare provider
Other informationInactive ingredients Questions or comments? 1-800-952-5080 www.orajel.com

Principal Display Panel

No 1 TEETHING BRAND
        used by Pediatricians

                                                        
                                            Orajel

                                         Instant Relief
                                       for Teething Pain

                                                                                                                cherry flavored gel

                                             

                                 
           LONGER LASTING                                                                            

NET WT 0.33 OZ (9.4g) Gel                     ORAL PAIN RELIEVER FOR TEETHING   BENZOCAINE 7.5%        

Carton imageOrajel Instant Relief for Teething Pain

Orajel Instant Relief for Teething Pain

Benzocaine GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10237-735
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BENZOCAINE Benzocaine 75 mg

Inactive Ingredients

Ingredient Name Strength
CARBOXYMETHYLCELLULOSE SODIUM
GELATIN
Mineral Oil
PECTIN
petrolatum
polyethylene glycol
FD&C RED NO. 40
saccharin sodium

Product Characteristics

Color
red

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10237-735-18 5.1 in 1 TUBE
2 3.5 in 1 TUBE
3 11.9 in 1 TUBE
4 9.4 in 1 TUBE
5 NDC:10237-735-33 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part356 2011-03-22


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Be sure to consult your doctor before taking any medication!
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