TIGER DELAYSPRAY- lidocaine spray

Tiger delayspray by

Drug Labeling and Warnings

Tiger delayspray by is a Otc medication manufactured, distributed, or labeled by Magverz INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Lidocaine HCI 10 % ... External Anesthetic

Purpose

External Anesthetic

Keep out of Reach of Children

WARNINGS: Keep out of reach of children.

For External use only 

Indication and Usage

temporarily reduces sensitivity of the penis, which helps to delay ejaculation in cases of over-rapid or premature ejaculation (coming to a climax too quickly)

Inactive Ingredients

Ethanol,Propyelene glycol, Vitamin E and Essence 

Warning

Allergy alert: do not use this product if you or your partner are allergic (sensitive) to local Anesthetics.

Do not use - on broken or inflamed skin -if your partner is pregnant

Ask a doctor before use if you have, or ever had, liver or kidney problems

Ask a doctor or pharmacist before use if you are already taking prescribed drugs

when using this product

- do not get into eyes

- do not inhale

- do not exceed 24 sprays in 24 hours

Dosage and Administration

-apply 3 or more sprays, not to exceed 10, to the head and shaft of the penis before intercourse, or as directed by a doctor

-wash product after intercourse

-correct quantity and time of application will be determined by individual requirements and you should always use the minimum effective quantity

Product Label

INGREDIENTS AND APPEARANCE

TIGER DELAYSPRAY 
lidocaine spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59240-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	10 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
STEARIC ACID (UNII: 4ELV7Z65AP)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59240-006-06	6 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/03/2017
2	NDC: 59240-006-08	8 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/03/2017
3	NDC: 59240-006-12	12 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/03/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part346	01/03/2017

Labeler - Magverz INC (078712269)

Registrant - Magverz INC (078712269)