YEAST GARD HOMEOPATHIC GEL HOMEOPATHIC GEL TREATMENT- borax, collinsonia canadensis, berberis vulgaris, hamamelis virginiana gel 
Wisconsin Pharmacal Company

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Active Ingredients

Borax 3X HPUS

Collinsonia Canadensis 3X HPUS

Berberis Vulgaris 6X HPUS

Hamamelis Virginiana 6X HPUS

Purpose Temporary relief from external vagianl discomfort including itching, burning, and irritation

Uses For temporary relief of symptoms associate with vaginal yeast infection, including:itching, burning, and irritation.

Warnings

For external vaginal use only. Use only as directed.

Keep out of reach of children. If swallowed, get medial help or contact a Poison Control Center right away. If in eyes, flush with water for 15 minutes and call a physician.

Stop use and ask 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, fever, chills, nausea, vomiting, or foul-smelling vaginal discharge.

Do not use if

  • you have never had a vaginal yeast infection diagnosed by a doctor.

When using this product

  • Wash hands thoroughly with soap and water before and after use
  • Avoid contact with eyes
  • If burning sensation occurs and lasts more than a few minutes, remove gel and discontinue use
  • Do not use more than one week unless directed by a doctor
  • If yoyu do not get complete relief ask a doctor before using another product.

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

If pregnant or breast-feeding, ask a health professional before use.

Directions

Directions

Inactive Ingredients

Allantoin, Benzalkonium Chloride 50%, Disodium EDTA, Glucono Delta Lactone, Polysorbate 20, Propanediol, Sodium Benzoate, Sodium Hydroxide, Tea Tree Oil, Water, Xanthan Gum

Other Information

Other information

Questions or comments? 1-800-635-3696

tubecarton

YEAST GARD HOMEOPATHIC GEL  HOMEOPATHIC GEL TREATMENT
borax, collinsonia canadensis, berberis vulgaris, hamamelis virginiana gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68093-7247
Route of AdministrationVAGINAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS) HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK6 [hp_X]  in 1 g
COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR) (COLLINSONIA CANADENSIS ROOT - UNII:O2630F3XDR) COLLINSONIA CANADENSIS ROOT3 [hp_X]  in 1 g
SODIUM BORATE (UNII: 91MBZ8H3QO) (BORATE ION - UNII:44OAE30D22) SODIUM BORATE3 [hp_X]  in 1 g
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK6 [hp_X]  in 1 g
Inactive Ingredients
Ingredient NameStrength
PROPANEDIOL (UNII: 5965N8W85T)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
ALLANTOIN, (+)- (UNII: XDK458E1J9)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
WATER (UNII: 059QF0KO0R)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
TEA TREE OIL (UNII: VIF565UC2G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68093-7247-11 in 1 CARTON04/01/2007
128.35 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic04/01/2007
Labeler - Wisconsin Pharmacal Company (800873986)
Establishment
NameAddressID/FEIBusiness Operations
Wisconsin Pharmacal Company800873986manufacture(68093-7247)

Revised: 12/2018
Document Id: 7c5d8463-52e0-a397-e053-2991aa0abc29
Set id: de4dc2a2-b829-4b1b-8813-94700315a7bc
Version: 2
Effective Time: 20181206
 
Wisconsin Pharmacal Company