VCF CONTRACEPTIVE PRE-FILLED APPLICATORS- nonoxynol-9 gel, metered 
APOTHECUS PHARMACEUTICAL CORP

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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VCF® CONTRACEPTIVE GEL PRE-FILLED APPLICATORS

Drug Facts

Active Ingredient

Nonoxynol-9, (4%)

Purpose

Vaginal Contraceptive

Use

Warnings

For Vaginal Use Only

Not for rectal (anal) use.

Sexually Transmitted Disease (STDs) alert

This product does not protect against HIV (AIDS) or other STDs and may increase the risk of getting HIV from an infected partner.

Do not use if you or your sex partner has HIV/AIDS. If you do not know if you or your sex partner is infected, choose another form of birth control

Stop use and ask a doctor if you or your partner get burning, itching, a rash, or other irritation of the vagina or penis.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other Information

Inactive Ingredients

purified water, propylene glycol, CMC 7MF, sorbitol solution, PVP K 30, simethicone, lactic acid, methyl paraben, potassium sorbate, sodium benzoate, trisodium EDTA

Questions?

If you have any questions, call our toll-free line at 1-800-879-2393 between 9:00AM and 5:00PM EST, Monday through Friday.

Distributed By:
Apothecus Pharmaceutical Corp.
Oyster Bay, NY 11771

PRINCIPAL DISPLAY PANEL - 2.55 g Applicator Box

New!

Compare To
CONCEPTROL®!

VCF®

Vaginal
Contraceptive
Gel

FOR PREVENTION OF PREGNANCY

Pre-Filled Applicators

Contains the Spermicide
Doctors Recommend Most

10
PRE-FILLED APPLICATORS
NET WT. 0.09 oz. (2.55g) EACH

PRINCIPAL DISPLAY PANEL - 2.55 g Applicator Box
VCF CONTRACEPTIVE PRE-FILLED APPLICATORS 
nonoxynol-9 gel, metered
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52925-512
Route of AdministrationVAGINAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NONOXYNOL-9 (UNII: 48Q180SH9T) (NONOXYNOL-9 - UNII:48Q180SH9T) NONOXYNOL-94 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Sodium Benzoate (UNII: OJ245FE5EU)  
Sorbitol (UNII: 506T60A25R)  
Povidone K30 (UNII: U725QWY32X)  
Lactic Acid, Unspecified Form (UNII: 33X04XA5AT)  
Methylparaben (UNII: A2I8C7HI9T)  
Potassium Sorbate (UNII: 1VPU26JZZ4)  
Edetate Trisodium (UNII: 420IP921MB)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52925-512-1010 in 1 BOX06/01/2014
12.55 g in 1 APPLICATOR; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2NDC:52925-512-25250 in 1 CARTON06/01/2014
22.55 g in 1 APPLICATOR; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333A06/01/2014
Labeler - APOTHECUS PHARMACEUTICAL CORP (119263747)

Revised: 1/2023
Document Id: d167d030-407a-4694-9211-7f2b5a27659f
Set id: 34be97cd-3646-427d-8112-ba0030ff8d88
Version: 5
Effective Time: 20230117
 
APOTHECUS PHARMACEUTICAL CORP