Pleasure Balm

Product NDC
56152-1470
11-digit product format
561521470
Labeler code
56152
Product ID
56152-1470_41249649-feb9-6694-e063-6294a90a13d2
Type
HUMAN OTC DRUG
Nonproprietary name
Benzocaine
Dosage form
GEL
Route
TOPICAL
Labeler
Cosmetic Enterprises Ltd
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2013-09-12
Substance
BENZOCAINE
Active strength
5 g/100mL
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
Pleasure Balm
Brand name suffix
Kama Sutra
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOCAINE5 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU3RSY48JW5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56152-1470-1Pleasure BalmKama Sutra12 mL in 1 TUBEGEL1219

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56152-1470PLEASURE BALM KAMA SUTRA (BENZOCAINE) GEL [COSMETIC ENTERPRISES LTD]18Current NDC, Legacy NDC, 1 package rows20241105_f370e3c4-65ca-4f3c-a5aa-70e198e681a2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
56152-1470-15615214700112 mL in 1 TUBE (56152-1470-1) 12 ml2018-12-130000-00-00NoNoCurrent