NDC | 68093-6661-1 |
Set ID | c348fb59-d711-4e9c-9b60-69e46cee831a |
Category | HUMAN OTC DRUG LABEL |
Packager | Wisconsin Pharmacal Company |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
-
WARNINGS
Warnings Use only as directed
Do not use if you have never had a vaginal yeast infection diagnosed by a doctor.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Stop use and ask a doctor if
- Symptoms worsen, last more than 7 days, or clear up and occur again within a few days
- You get a rash or hives, abdominal pain, lever, chills, nausea, vomiting, or foul-smelling vaginal discharge.
Ask a doctor before use if you have:
- Vaginal itching and discomfortlor the first time
- Lower abdominal, back or shoulder pain, fever, chills, nausea, vomiting, ortoul-smelling vaginal discharge. You may have a more
serious condition.
- Vaginal yeast infections often [such as once a month or 3 in 5 months). You could be pregnant or have a serious underlying medical cause lor your symptoms, including diabetes or a weakened immune system.
- Been exposed to the human immunodeficiency virus (Hill) that causes AIDS
- You have an STD (sexually transmitted disease) or PID (pelvic inflammatory disease)
- You have frequent and painful urination.
- DOSAGE & ADMINISTRATION
-
OTHER SAFETY INFORMATION
Other information
- Do not use if safety seal under cap is missing or broken
- Store at room temperature
- Lot number and expiration date: see side ol box.
There is no scientific evidence that this product works. The product claims are based on theories of
homeopathy from the 1700's that are not accepted by most modern medical experts. - INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
YEAST GARD ADVANCED TREATS AND PREVENTS SYMPTOMS OF VAGINAL YEAST INFECTIONS
collinsonia canadensis, kali muriaticum, calcarea carbonica capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68093-6661 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 6 [hp_X] COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR) (COLLINSONIA CANADENSIS ROOT - UNII:O2630F3XDR) COLLINSONIA CANADENSIS ROOT 3 [hp_X] POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE 3 [hp_X] Inactive Ingredients Ingredient Name Strength MAGNESIUM STEARATE (UNII: 70097M6I30) BROWN RICE (UNII: 659G217HPG) BACILLUS COAGULANS (UNII: ISK1LOY57E) GELATIN (UNII: 2G86QN327L) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color white (off white) Score no score Shape OVAL (Capsule) Size 20mm Flavor Imprint Code LPC;HMI Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68093-6661-1 1 in 1 CARTON 04/01/2007 1 60 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/01/2007 Labeler - Wisconsin Pharmacal Company (800873986) Establishment Name Address ID/FEI Business Operations Wisconsin Pharmacal Company 800873986 manufacture(68093-6661)