NDC | 68093-7106-1 |
Set ID | b3f066d9-0f0f-455d-b1b1-dc13ba80fbfc |
Category | HUMAN OTC DRUG LABEL |
Packager | Wisconsin Pharmacal Company |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
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Warnings
For vaginal use only. Use only as directed.
Do not use if you have never had a vaginal yeast infection diagnosed by a doctor.
Stop use and ask a doctor if:
- Symptoms last more than 7 days
- You get a rash or hives, abdominal pain, fever, chills, nausea, vomiting, or foul-smelling vaginal discharge.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Ask a doctor before use if you have
- Vaginal itching and discomfort for the first time
- Lower abdominal, back or shoulder pain, fever, chills, nausea, vomiting, or foul-smelling vaginal discharge. You may have a serious condition.
- Vaginal yeast infections often (such as once a month or 3 in 6 months). You could be pregnant or have a serious underlying medical cause for you symptoms, including diabetes or a weakened immune system.
- Been exposed to the human immunodeficiency virus (HIV) that causes AIDS
- You have an STD (sexually transmitted disease) or PID (Pelvic inflammatory disease)
- You have frequent and painful urination
- Directions
- Other information
- Inactive Ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
YEAST GARD ADVANCED
borax, collinsonia canadensis, berberis vulgaris, hamamelis virginiana suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68093-7106 Route of Administration VAGINAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 6 [hp_X] SODIUM BORATE (UNII: 91MBZ8H3QO) (BORATE ION - UNII:44OAE30D22) SODIUM BORATE 3 [hp_X] COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR) (COLLINSONIA CANADENSIS ROOT - UNII:O2630F3XDR) COLLINSONIA CANADENSIS ROOT 3 [hp_X] HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS) HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 6 [hp_X] Inactive Ingredients Ingredient Name Strength POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) BACILLUS COAGULANS (UNII: ISK1LOY57E) POLYETHYLENE GLYCOL 1450 (UNII: OJ4Z5Z32L4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68093-7106-1 10 in 1 CARTON 05/01/2008 1 1 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/01/2008 Labeler - Wisconsin Pharmacal Company (800873986) Establishment Name Address ID/FEI Business Operations Wisconsin Pharmacal Company 800873986 manufacture(68093-7106)