Naughty Kitty Kat

Product NDC
84243-211
11-digit product format
842430211
Labeler code
84243
Product ID
84243-211_46552bd8-124f-bbd8-e063-6394a90a0585
Type
HUMAN OTC DRUG
Nonproprietary name
No Gag Deep Throat Spray
Dosage form
SPRAY
Route
ORAL
Labeler
INKED SUGAR, INC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-04-27
Substance
BENZOCAINE; GLYCERIN
Active strength
3; 30 mg/100mL; mg/100mL
Pharmacologic classes
Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Naughty Kitty Kat
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOCAINE3 mg/100mL
GLYCERIN30 mg/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
U3RSY48JW5Internal UNII lookup
PDC6A3C0OXInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
170eb644-c72c-5744-e063-6394a90a767dAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84243-211-11Naughty Kitty Kat30 mL in 1 BOTTLE, SPRAYSPRAY302

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 145 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
INTIMALE Maximum Strength DelayLIDOCAINE HYDROCHLORIDESKINS SEXUAL HEALTH LIMITED25b9ade3-72b0-4b86-8c48-90310a26806f2023-11-11WarningsExact identifier
application number: M017
POWERECT Max Power Male DelayLIDOCAINE HYDROCHLORIDESKINS SEXUAL HEALTH LIMITED25a1c926-9543-44a7-865e-a4b6e1a40cbe2023-11-11WarningsExact identifier
application number: M017
SKINS DELAY Maximum Strength LidocaineLIDOCAINE HYDROCHLORIDESKINS SEXUAL HEALTH LIMITED172efe5d-28b8-443c-b3f9-4296691890812023-11-11WarningsExact identifier
application number: M017
GASPARI Ageless Pain Relief CreamMENTHOLGASPARI ANTI-AGING LLCea806089-688b-4944-ad69-86f366509eb52023-11-11WarningsExact identifier
application number: M017
ZENSEZONE Arthmed Temporary Pain Relief CreamCAPSAICIN, MENTHOL, METHYL SALICYLATEZENSEZONE LLCc5778f22-c411-4bd7-b2af-45e3fee15fd22023-11-11WarningsExact identifier
application number: M017
PRFC HEMP Topical AnalgesicMENTHOLDOBEST INC722da9d1-91d7-45be-adb1-8d6a22aa83ac2023-11-11WarningsExact identifier
application number: M017
AMP RELIEF Pain Relief CreamMENTHOLCOASTAL FORMULAS LLC84ea496e-ab54-4882-93ef-600f8eb33cb42023-11-11WarningsExact identifier
application number: M017
AMP RELIEF Pain Relief CreamMENTHOLCOASTAL FORMULAS LLC39564c67-49ab-42d4-a391-792ac69180c02023-11-11WarningsExact identifier
application number: M017
LIDOSOLVE PAIN RELIEFLIDOCAINE HYDROCHLORIDEHENNIKA HEALTH, LLC3a9e4e0c-362d-4e66-bb5f-984fe1c9d4e22023-11-11WarningsExact identifier
application number: M017
AMINO ACTIVE Topical Analgesic CreamHISTAMINE DIHYDROCHLORIDEVIREO SYSTEMS, INC.591b1e7e-a8c0-4640-a592-4e0f3538a40e2023-11-11WarningsExact identifier
application number: M017
NERVE ACTIVE Pain Relief CreamMENTHOLTOP DOG DIRECT, LLCa8b85dcb-fd3e-4340-a945-609fc741443c2023-11-11WarningsExact identifier
application number: M017
GeriGentle FrostyHeat Pain Relief Patch 4 Lodocaine BackLIDOCAINEGeri-Gentle Corporatione4427928-c063-9ca6-e053-2995a90a1aa12023-11-10WarningsExact identifier
application number: M017
GeriGentle FrostyHeat Pain Relief Patch Arm and NeckMENTHOLGeri-Gentle Corporatione4429f70-667e-662b-e053-2a95a90a62ba2023-11-10WarningsExact identifier
application number: M017
GeriGentle FrostyHeat Pain Relief Patch BackMENTHOLGeri-Gentle Corporatione442b8ec-a3de-65e8-e053-2995a90af3ec2023-11-10WarningsExact identifier
application number: M017
SUPER WHITE STUFF Pain ReliefMENTHOLBLUE SPRING WELLNESS, L.L.C.9f948fb4-4275-4a1f-83f8-cd708db4a2962023-11-10WarningsExact identifier
application number: M017
SUPER WHITE STUFF PAIN RELIEFMENTHOLBLUE SPRING WELLNESS, L.L.C.b4278b70-e9a6-4d1f-bbad-257fe437b86a2023-11-10WarningsExact identifier
application number: M017
BLUE SPRING Foot and Leg Comfort Cream with Pain ReliefMENTHOL, CAPSAICINBLUE SPRING WELLNESS, L.L.C.2f9cf514-48be-49ec-b424-0b228b4b874a2023-11-10WarningsExact identifier
application number: M017
SUPER WHITE STUFF Pain ReliefMENTHOLBLUE SPRING WELLNESS, L.L.C.1231ddd2-7661-45b2-ab15-32f7fdc078a82023-11-10WarningsExact identifier
application number: M017
SUPER WHITE Stuff Pain ReliefMENTHOLBLUE SPRING WELLNESS, L.L.C.7779b26b-ae3b-4639-a6b0-826c7ab37a862023-11-10WarningsExact identifier
application number: M017
Alo Therapeutic MassageMENTHOL, HISTAMINE DIHYDROCHLORIDETheraplex Solutionsa898d2ef-5fa0-4144-8bb5-f6d5fc3ff0d42023-11-10WarningsExact identifier
application number: M017

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84243-211-118424302111130 mL in 1 BOTTLE, SPRAY (84243-211-11) 30 ml2024-04-27NoNoCurrent