Red Cross Toothache

Manufacturer
The Mentholatum Company
Effective date
2025-06-11
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-06-01 01:17:04

Label at a glance#

ProductRed Cross Toothache
Active ingredientEUGENOL
Label structure10 sections

Indications and uses

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

Dosage and administration

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 minute without 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 dent...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Eugenol 85%

Purpose

OTC - PURPOSE SECTION

Toothache relief agent

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

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

When using this product

OTC - WHEN USING SECTION

  • 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

OTC - STOP USE SECTION

  • 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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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 minute without 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

INACTIVE INGREDIENT SECTION

sesame oil

Questions

OTC - QUESTIONS SECTION

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

Package Label/Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FrontFrontPackage Label Principal Display Panel

Package Label/Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BackBackPackage Label Principal Display Panel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
EUGENOL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130310742000917GTIN-13: 0310742000917
EAN-13: 0310742000917
GTIN-12: 310742000917
UPC-A: 310742000917
GTIN storage (14 digits): 00310742000917
Image 2_Back.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10742-0009-12023-02-07C16284748780-1f386c649-a9ab-0266-e053-dadaa90a7c1aDrug Facts - Red Cross Toothache
10742-0009-12023-01-30C16284748780-1f386c649-a9ab-0266-e053-dadaa90a7c1aDrug Facts - Red Cross Toothache

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10742-0009-1Red Cross Toothache3.7 mL in 1 BOTTLELIQUID3.710
10742-0009-1Red Cross Toothache1 in 1 BLISTER PACKLIQUID110

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
EUGENOLACTIVE INGREDIENT3T8H1794QW2
EUGENOLACTIVE MOIETY3T8H1794QW2
SESAME OILINACTIVE INGREDIENTQX10HYY4QV2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10742-000910742-0009-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
SESAME OILQX10HYY4QVIACT
EUGENOL3T8H1794QWACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SESAME OILSESAME OILQX10HYY4QVINJECTION / INTRAMUSCULAR70 %v/vExact identifier — unii candidate
4 equally ranked IID candidates
SESAME OILSESAME OILQX10HYY4QVINJECTION / INTRAMUSCULAR70 %v/vExact identifier — unii candidate
4 equally ranked IID candidates
SESAME OILSESAME OILQX10HYY4QVCAPSULE / ORAL2325 mgExact identifier — unii candidate
4 equally ranked IID candidates
SESAME OILSESAME OILQX10HYY4QVCAPSULE / ORAL2325 mgExact identifier — unii candidate
4 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Red Cross ToothacheEUGENOLThe Mentholatum Company3537e599-65d9-48d6-8a46-d42312f71e842025-06-11WarningsExact identifier
ndc (package): 10742-0009-1
ndc (product): 10742-0009
ndc11 (package): 10742000901
spl id: 37516e9a-d5c4-496b-e063-6394a90a4c98
spl set id: 3537e599-65d9-48d6-8a46-d42312f71e84

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.