UltraCare Anesthetic Gel

Product NDC
10129-071
11-digit product format
101290071
Labeler code
10129
Product ID
10129-071_2ce062b9-3d84-7918-e063-6294a90acdfe
Type
HUMAN OTC DRUG
Nonproprietary name
Benzocaine
Dosage form
GEL
Route
DENTAL; PERIODONTAL; TOPICAL
Labeler
The Bellport Company, Inc. dba Gingi-Pak
Application
M022
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-02-08
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

Additional Listing Data#

Finished product
Yes
Brand name base
UltraCare Anesthetic Gel
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
10129-071-01UltraCare Anesthetic Gel30 g in 1 BOTTLEGEL302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10129-071ULTRACARE ANESTHETIC GEL (BENZOCAINE) GEL [THE BELLPORT COMPANY, INC. DBA GINGI-PAK]2Current NDC, 1 package rows20250130_f5dd8fa8-0b6a-5a30-e053-2995a90ad194.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
238910benzocaine 20 % Oral GelPSNf5dd8fa8-0b6a-5a30-e053-2995a90ad1942
238910benzocaine 0.2 MG/MG Oral GelSCDf5dd8fa8-0b6a-5a30-e053-2995a90ad1942
238910benzocaine 20 % (180-220 MG per 1 GM) Oral GelSYf5dd8fa8-0b6a-5a30-e053-2995a90ad1942

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
10129-071-011012900710130 g in 1 BOTTLE (10129-071-01) 30 g2023-02-08NoNoCurrent