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.

----------

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

Labeling

10 spray

Labeling

20 spray

Labeling

40 spray

Labeling

60 spray

PROMESCENT 
lidicaine spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55636-590
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Lidocaine (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) Lidocaine10 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55636-590-741 in 1 CARTON01/11/2013
17.4 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
2NDC:55636-590-131 in 1 CARTON01/11/2013
21.3 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
3NDC:55636-590-261 in 1 CARTON01/11/2013
33.8 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
4NDC:55636-590-521 in 1 CARTON01/11/2013
45.4 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34801/11/2013
Labeler - Absorption (014937753)
Registrant - Swiss-American CDMO, LLC (080170933)
Establishment
NameAddressID/FEIBusiness Operations
Swiss-American CDMO, LLC080170933manufacture(55636-590) , label(55636-590) , pack(55636-590)

Revised: 3/2021
Document Id: 7f289f51-0f0a-413c-935c-9fddf59a94a4
Set id: 5b508238-3be7-4b0d-bf35-51de79f58f55
Version: 4
Effective Time: 20210325
 
Absorption