PROMESCENT- lidicaine spray 
Absorption

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Promescent

Active Ingredient (per spray)

Lidocaine approx. 10mg

Purpose

Anesthetic

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Use:

Helps in temporarily slowing the onset of ejaculation.

Warnings:

​For external use only.

​Do not use if

​Ask a doctor or pharmacist before use if

​When using this product

​Stop use and ask a doctor

Directions:

Break front tab first. To unlock, press in special Child Resistant (R) tab in back of the actuator while turning the actuator to the right. Press the actuator down repeatedly until product dispenses to prime spray pump. Apply 3 or more sprays, not to exceed 10, to head and shaft of penis 10 minutes before sexual intercourse, or use as directed by a doctor. Recommended Initial Dosage: 3 sprays. Rub Promescent into the skin of the penis until all of the product is absorbed. Wash product off after intersourse. After spraying, turn actuator to the left to lock.

Inactive Ingredients:

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Ceteareth-20, Cetearyl Alcohol, Citric Acid, Dimethicone, Farnesol, Fragrance, Glycerin, Hydrogenated Polyisobutene, Macadamia Ternifolia Seed Oil, Panthenol, Phenoxyethanol, Purified Water (Aqua), SD Alcohol 40-B, Sodium Hydroxide, Soy Lecithin, Stearoxytrimethylsilane, Stearyl Alcohol, Thymol, Tocopheryl Acetate (Vitamin E).

Labeling

Label

Unit Carton

PROMESCENT 
lidicaine spray
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:55636-590
Route of Administration TOPICAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Lidocaine (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) Lidocaine 10 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
GLYCERIN (UNII: PDC6A3C0OX)  
PANTHENOL (UNII: WV9CM0O67Z)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)  
STEAROXYTRIMETHYLSILANE (UNII: 9862TW94B2)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
MACADAMIA OIL (UNII: 515610SU8C)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
FARNESOL (UNII: EB41QIU6JL)  
THYMOL (UNII: 3J50XA376E)  
ALCOHOL (UNII: 3K9958V90M)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:55636-590-74 1 in 1 CARTON
1 7.4 g in 1 BOTTLE, SPRAY
2 NDC:55636-590-13 1 in 1 CARTON
2 1.3 g in 1 BOTTLE, SPRAY
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part348 01/11/2013
Labeler - Absorption (014937753)
Registrant - Ei Inc. (105803274)
Establishment
Name Address ID/FEI Business Operations
Ei Inc. 105803274 manufacture(55636-590) , label(55636-590) , pack(55636-590)

Revised: 1/2013
Document Id: 4ae9e446-dfbe-4163-9a8b-7d75c1f501f4
Set id: 5b508238-3be7-4b0d-bf35-51de79f58f55
Version: 1
Effective Time: 20130116
 
Absorption