FDA.reportPublic FDA data

Orajel Rescue Relief Pen

Product NDC
10237-731
11-digit product format
102370731
Labeler code
10237
Product ID
10237-731_38d791e8-33d3-22e4-e063-6394a90aff90
Type
HUMAN OTC DRUG
Nonproprietary name
Oral Pain Reliever
Dosage form
GEL
Route
ORAL
Labeler
Church & Dwight Co., Inc.
Application
M022
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-02-01
Substance
BENZOCAINE; MENTHOL; ZINC CHLORIDE
Active strength
200; 2.6; 1.5 mg/g; mg/g; mg/g
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [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
Orajel Rescue Relief Pen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOCAINE200 mg/g
MENTHOL2.6 mg/g
ZINC CHLORIDE1.5 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU3RSY48JW5, L7T10EIP3A, 86Q357L16B
Rxcui2362013

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10237-731-07Orajel Rescue Relief Pen1 in 1 BLISTER PACKGEL12
10237-731-07Orajel Rescue Relief Pen2 g in 1 APPLICATORGEL22
10237-731-27Orajel Rescue Relief Pen1 in 1 BLISTER PACKGEL12
10237-731-27Orajel Rescue Relief Pen2 in 1 PACKAGEGEL22

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10237-731ORAJEL RESCUE RELIEF PEN (ORAL PAIN RELIEVER) GEL [CHURCH & DWIGHT CO., INC.]1Current NDC, 4 package rows20250207_2d68eec5-ae8a-9cdf-e063-6294a90a9799.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2362013benzocaine 20 % / menthol 0.26 % / zinc chloride 0.15 % Oral GelPSN2d68eec5-ae8a-9cdf-e063-6294a90a97992
2362013benzocaine 0.2 MG/MG / menthol 0.0026 MG/MG / zinc chloride 0.0015 MG/MG Oral GelSCD2d68eec5-ae8a-9cdf-e063-6294a90a97992
2362013benzocaine 20 % / menthol 0.26 % / zinc chloride 0.15 % Oral GelSY2d68eec5-ae8a-9cdf-e063-6294a90a97992

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
10237-731-07102370731071 APPLICATOR in 1 BLISTER PACK (10237-731-07) / 2 g in 1 APPLICATOR1 applicator2025-02-01NoNoCurrent
10237-731-27102370731272 BLISTER PACK in 1 PACKAGE (10237-731-27) / 1 APPLICATOR in 1 BLISTER PACK / 2 g in 1 APPLICATOR2 blister pack2025-06-01NoNoCurrent