ANAL BLU- desensitizer cream

Anal Blu by

Drug Labeling and Warnings

Anal Blu 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 BLU 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, FD&C Blue #1

Anal Blu

Anal Blu

EUROPEAN FORMULATED ANAL-ESE

Anal Blu Pineapple-Cherry Flavor

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 BLU 
desensitizer cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83608-108
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 BLUE NO. 1 (UNII: H3R47K3TBD)
PEG-75 STEARATE (UNII: OT38R0N74H)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83608-108-05	1 in 1 CARTON	08/07/2023
1		0.5 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 83608-108-15	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(83608-108)