RED CROSS TOOTHACHE- eugenol liquid

Red Cross Toothache by

Drug Labeling and Warnings

Red Cross Toothache by is a Otc medication manufactured, distributed, or labeled by The Mentholatum Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Eugenol 85%

Purpose

Toothache relief agent

Uses

temporarily relieves throbbing, persistent toothache due to a cavity until a dentist can be seen

Warnings

For external use only

Allergy alert: do not use if you are allergic to eugenol (clove oil)

When using this product

• use only in teeth with persistent, throbbing pain
• avoid touching tissues other than tooth cavity. Contact with lips or mucous membranes can cause burning, swelling, or irritation.
• DO NOT SWALLOW to avoid irritation
• do not use for more than 7 days
• do not exceed recommended dosage

Stop use and ask a dentist or doctor if

• irritation persists, inflammation develops, or if fever and infection develop

See a dentist as soon as possible whether or not the pain is relieved. Toothaches and open cavities indicate serious problems that need prompt attention by a dentist.

Keep Out of Reach of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• rinse tooth with water to remove any food particles from the cavity
• using tweezers, immerse cotton pellet in medication
• to prevent dripping, squeeze gently between fingers to remove excess liquid
• place pellet in tooth cavity for one minutewithout touching surrounding tissues, then remove
• supervise children using this product

adults and children 12 years and over: use up to 4 times daily or as directed by a dentist or doctor

children under 12 years: ask a dentist or doctor

Inactive Ingredients

sesame oil

Questions

1-877-636-2677 MON-FRI 9 AM to 5 PM (EST)

Package/Label Principal Display Panel

Principal Display Panel

INGREDIENTS AND APPEARANCE

RED CROSS TOOTHACHE 
eugenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10742-0009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EUGENOL (UNII: 3T8H1794QW) (EUGENOL - UNII:3T8H1794QW)	EUGENOL	850 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SESAME OIL (UNII: QX10HYY4QV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10742-0009-1	1 in 1 BLISTER PACK	06/21/1983
1		3.7 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part356	06/21/1983

Labeler - The Mentholatum Company (002105757)

Registrant - The Mentholatum Company (002105757)

Establishment
Name	Address	ID/FEI	Business Operations
The Mentholatum Company		002105757	MANUFACTURE(10742-0009)