Dental City Topical Anesthetic

Product NDC
69483-008
11-digit product format
694830008
Labeler code
69483
Product ID
69483-008_2b49f56a-c4fb-eee2-e063-6294a90a9e75
Type
HUMAN OTC DRUG
Nonproprietary name
Benzocaine
Dosage form
GEL
Route
DENTAL
Labeler
ICP Inc DBA Dental City
Application
M022
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2014-04-01
Substance
BENZOCAINE
Active strength
200 mg/g
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dental City Topical AnestheticBENZOCAINEICP Inc DBA Dental Cityfba82d55-94db-4432-b532-603fe57202be2025-01-09WarningsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings

Warnings Methemoglobinemia warning: Use of this product may cause methemoglobinemia, a serious condition that must be treated promptly because it reduces the amount of oxygen carried in the blood. This can occur even if you have used this product before. Stop use and seek immediate medical attention if you or a child in your care develops: pale, gray or blue colored skin (cyanosis) headache rapid heart rate shortness of breath dizziness or lightheadedness fatigue or lack of energy Allergy Alert: Do not use on patients with a history of allergies to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics. Do not use for more than 7 days unless directed by a physician. If sore mouth symptoms do not improve in 7 days; irritation, pain, or redness persists or worsens; or if swelling, rash or fever develops, see your physician promptly. for teething in children under 2 years of age When using this product Avoid contact with eyes. If contact occurs, flush with water. Do not exceed recommended dosage. If more than used for pain is accidentally swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast feeding, ask a physician before use.

Additional Listing Data#

Finished product
Yes
Brand name base
Dental City Topical Anesthetic
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOCAINE200 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU3RSY48JW5
Rxcui238910

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69483-008-30Dental City Topical Anesthetic30 g in 1 JARGEL304

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69483-008DENTAL CITY TOPICAL ANESTHETIC (BENZOCAINE) GEL [ICP INC DBA DENTAL CITY]4Current NDC, Legacy NDC, 1 package rows20250112_fba82d55-94db-4432-b532-603fe57202be.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
238910benzocaine 20 % Oral GelPSNfba82d55-94db-4432-b532-603fe57202be4
238910benzocaine 0.2 MG/MG Oral GelSCDfba82d55-94db-4432-b532-603fe57202be4
238910benzocaine 20 % (180-220 MG per 1 GM) Oral GelSYfba82d55-94db-4432-b532-603fe57202be4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69483-008-306948300083030 g in 1 JAR (69483-008-30) 30 g2018-10-010000-00-00NoNoCurrent