Walgreens Pain Relief

Product NDC
0363-5061
11-digit product format
003635061
Labeler code
0363
Product ID
0363-5061_b305fced-9c43-464a-b813-2fc790d0df1c
Type
HUMAN OTC DRUG
Nonproprietary name
BENZOCAINE
Dosage form
GEL
Route
ORAL
Labeler
Walgreens Company
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2013-03-19
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
Walgreens Pain Relief
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
0363-5061-33Walgreens Pain Relief1 in 1 CARTONGEL12
0363-5061-33Walgreens Pain Relief9.35 g in 1 TUBEGEL9.352

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-5061WALGREENS PAIN RELIEF (BENZOCAINE) GEL [WALGREENS COMPANY]2Current NDC, Legacy NDC, 2 package rows20241122_7cee7234-32cd-4bf3-8a6c-0882585eec7f.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
238910benzocaine 20 % Oral GelPSN7cee7234-32cd-4bf3-8a6c-0882585eec7f2
238910benzocaine 0.2 MG/MG Oral GelSCD7cee7234-32cd-4bf3-8a6c-0882585eec7f2
238910benzocaine 20 % (180-220 MG per 1 GM) Oral GelSY7cee7234-32cd-4bf3-8a6c-0882585eec7f2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0363-5061-33003635061331 TUBE in 1 CARTON (0363-5061-33) / 9.35 g in 1 TUBE1 tube2013-03-190000-00-00NoNoCurrent