Label: VCF CONTRACEPTIVE- nonoxynol-9 film, soluble
- NDC Code(s): 52925-112-01
- Packager: APOTHECUS PHARMACEUTICAL CORP.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 13, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each film)
- Purpose
- Use
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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
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Directions
- before using this product, read the enclosed package insert for complete directions and information
- be sure your fingers are dry before touching the film
- insert one film and place as far into the vagina as possible against the cervix
- insert VCF® not less than 15 minutes and not more than 3 hours before intercourse
- use one film before each act of intercourse
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Other information
- When used correctly every time you have sex, latex condoms greatly reduce, but do not eliminate, the risk of catching or spreading HIV, the virus that causes AIDS.
- Use a latex condom without nonoxynol-9 if you or your sex partner has HIV/AIDS, multiple sex partners, or other HIV risk factors.
- VCF® is tested by independent laboratories for determination of sperm inactivating qualities, using the I.P.P.F. agreed protocol
- Store at 58° - 86°F (15°-30°C)
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 9 x 1 Film Pouch Box
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INGREDIENTS AND APPEARANCE
VCF CONTRACEPTIVE
nonoxynol-9 film, solubleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52925-112 Route of Administration VAGINAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NONOXYNOL-9 (UNII: 48Q180SH9T) (NONOXYNOL-9 - UNII:48Q180SH9T) NONOXYNOL-9 280 mg Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) WATER (UNII: 059QF0KO0R) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52925-112-01 9 in 1 BOX 06/01/1988 1 1 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug 505G(a)(3) 06/01/1988 Labeler - APOTHECUS PHARMACEUTICAL CORP. (119263747)
