NAUGHTY KITTY KAT- no gag deep throat spray spray

Naughty Kitty Kat by

Drug Labeling and Warnings

Naughty Kitty Kat by is a Otc medication manufactured, distributed, or labeled by INKED SUGAR, INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Benzocaine 3% ................. Desensitizer Glycerin 30% ...................... Demulcent

Purpose

Desensitizer Demulcent

Use

For occasional personal use to help prevent the gag reflex

Warnings

Methemoglobinemia warning:

Use of this product may cause methemoglobinemia, a serious condition that must be treated promptly because it reduces the amount of oxygen carried in the blood. This can occur even if you have used this product before. Stop use and seek immediate medical attention if you or a child in your care develops pale, gray, or blue-colored skin (cyanosis), headache rapid heart rate, shortness of breath, dizziness or lightheadedness, fatigue or lack of energy

This product is not a contraceptive and contains no spermicide.

WHEN USING

Avoid contact with the eyes. Do not use an irritated or infected skin.

KEEP OUT OF REACH OF CHILDREN

Keep away from children.

STOP USE

adults 18 years of age and older: Apply 2-3 sprays to the back of the throat. Limit use to 3-4 times per day. For adults only. Not for sale to minors.

Directions

Adults: Before applying this product, gently dry the application area by patting or blotting it with toilet tissue or a clean, soft cloth.

Apply up to 6 times daily. Children under 12 years: consult a doctor.

Other information

Store at 20-25°C (68-77°F)

Inactive ingredients

Alcohol, Purifi ed Water, Acesulfame Potassium, Sucralose, Nat. & Art. Flavors, Citric Acid, Potassium Sorbate, Sodium Benzoate

Package Label - Principal Display Panel

30mL NDC: 84243-211-11

INGREDIENTS AND APPEARANCE

NAUGHTY KITTY KAT 
no gag deep throat spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84243-211
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	3 mg  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	30 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SUCRALOSE (UNII: 96K6UQ3ZD4)
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
ALCOHOL (UNII: 3K9958V90M)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84243-211-11	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/27/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/27/2024

Labeler - INKED SUGAR, INC (829149603)