NDC | 52925-312-06, 52925-312-14 |
Set ID | f7a7b388-e55e-4f55-b271-0a60bb7aa694 |
Category | HUMAN OTC DRUG LABEL |
Packager | APOTHECUS PHARMACEUTICAL CORP |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333A |
- SPL UNCLASSIFIED SECTION
- Active ingredient
- 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
Stop use and ask a Doctor if you or your partner get burning, itching, a rash, or other irritation of the vagina or penis
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Directions
- before using this product, read the enclosed package insert for complete directions and information
- insert one applicator full of foam in the vagina no more than one hour before each act of intercourse
- if this product is used together with another contraceptive method, there will probably be better protection against pregnancy
- if douching is desired, always wait at least 6 hours after intercourse before douching
- see enclosed instructions for cleaning the applicator after each use
- Other Information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 17 g Can Box
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INGREDIENTS AND APPEARANCE
VCF CONTRACEPTIVE
nonoxynol-9 aerosol, foamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52925-312 Route of Administration VAGINAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NONOXYNOL-9 (UNII: 48Q180SH9T) (NONOXYNOL-9 - UNII:48Q180SH9T) NONOXYNOL-9 125 mg in 1 g Inactive Ingredients Ingredient Name Strength BENZOIC ACID (UNII: 8SKN0B0MIM) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) CETYL ALCOHOL (UNII: 936JST6JCN) ACETIC ACID (UNII: Q40Q9N063P) METHYLPARABEN (UNII: A2I8C7HI9T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52925-312-14 1 in 1 BOX 06/01/1997 1 17 g in 1 CAN; Type 0: Not a Combination Product 2 NDC:52925-312-06 17 g in 1 CAN; Type 0: Not a Combination Product 06/01/1997 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333A 06/01/1997 Labeler - APOTHECUS PHARMACEUTICAL CORP (119263747)