ANAL-ESE- desensitizer cream

ANAL-ESE by

Drug Labeling and Warnings

ANAL-ESE by is a Otc medication manufactured, distributed, or labeled by Novelties by Nasswalk, Inc., Advance Cosmetics Research Laboratories Inc,. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient:

Benzocaine 7.5%

Purpose:

Desensitizer

Uses:

Desensitizing Lubricant. Where less painful anal penetration is desired.

Warnings:

For External use only. Do not use near eyes. Not for prolonged use. If condition for which preparation is used causes discomfort, or if a rash or irritation should develop, discontinue use and consult a physician. For prevention of premature ejaculation.

Keep out of reach of children.

Directions:

Apply a small amount of ANAL-ESE to rectal area prior to penetration. Wait a few minutes for desensitization before attempting penetration. Proper amount and waiting time will be determined after seferal uses.

Inactive Ingredients:

PEG-8, Glycerin, PEG-75, Sodium Saccharin, Flavor, Red 40

ANAL-ESE Strawberry Flavored

ANAL-ESE

STRAWBERRY

Exciting New Flavor

THE Original

Net Weight 1.5 oz.

Distributed By: Novelties by Nasswalk Inc, North Bergeb, NJ 07047. WWW.NASSTOYS.COM

1.5 Carton

1.5 Tube

Net Weight 0.5 oz.

Distributed By: Novelties by Nasswalk Inc, North Bergeb, NJ 07047. WWW.NASSTOYS.COM

0.5 Carton

0.5 Tube

INGREDIENTS AND APPEARANCE

ANAL-ESE 
desensitizer cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83608-107
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	7.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
PEG-8 STEARATE (UNII: 2P9L47VI5E)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
FD&C RED NO. 40 (UNII: WZB9127XOA)
PEG-75 STEARATE (UNII: OT38R0N74H)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83608-107-05	1 in 1 CARTON	08/07/2023
1		0.5 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 83608-107-15	1 in 1 CARTON	08/07/2023
2		1.5 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	08/07/2023

Labeler - Novelties by Nasswalk, Inc. (049455157)

Registrant - Novelties by Nasswalk, Inc. (049455157)

Establishment
Name	Address	ID/FEI	Business Operations
Advance Cosmetics Research Laboratories Inc,		874810872	manufacture(83608-107)