Label: EQUATE YEAST RELIEF- candida albicans, wood creosote, sodium chloride, and sulfur tablet
- NDC Code(s): 79903-094-14
- Packager: WAL-MART STORES INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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.
Drug Label Information
Updated December 31, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
-
Purpose
Candida albicans 30X - Relief from vaginal itching, burning and discharge
Candida albicans 30X - Relief from vaginal itching, burning, odor and discharge
Kreosotum 30X - Relief from vaginal itching, burning, odor and discharge
Natrium muriaticum 12X - Relief from vaginal itching, burning, odor and discharge
Sulphur 12X - Relief from vaginal itching, burning, odor and discharge
-
Uses
See your doctor if this is the first time you have vaginal itching and discomfort to find out if you have a vaginal yeast infection. According to homeopathic indications, these ingredients provide temporary relief of yeast infection related symprtoms such as:
- itching and burning, occasional vaginal odor and discharge, after consultation by a physician.
*These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
- Warnings
- Stop use and contact your physician if
- Ask Doctor
- Pregnancy warning
- Keep out of reach of children
-
Directions
Adults: take one tablet orally three times a day as long as symptoms persist. Children: consult a doctor prior to use.
- Take at least 10 minutes before or at least 10 minutes after eating or drinking.
- For occasional support take one tablet per day.
- Homeopathic remedies may not be effective for everyone. Individual results may vary.
-
Other Information
- Do not use if blister seal is broken.
- Store at 15° to 30°C (59° to 86° F).
- Active ingredients are micro-diluted in accordance with the Hemeopathic Pharmacopoeia of the United States and are therefore non-toxic with no known side effects or contraindications. Tamper evident: tablets sealed in blisters. Do not use if blister is open or damaged.
- Inactive Ingredients
- Questions or comments
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
EQUATE YEAST RELIEF
candida albicans, wood creosote, sodium chloride, and sulfur tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-094 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 30 [hp_X] WOOD CREOSOTE (UNII: 3JYG22FD73) (WOOD CREOSOTE - UNII:3JYG22FD73) WOOD CREOSOTE 30 [hp_X] SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 12 [hp_X] SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 12 [hp_X] Inactive Ingredients Ingredient Name Strength CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) SUCROSE (UNII: C151H8M554) MAGNESIUM STEARATE (UNII: 70097M6I30) Product Characteristics Color white Score score with uneven pieces Shape ROUND Size 10mm Flavor Imprint Code H Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-094-14 60 in 1 BOX 03/04/2022 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/04/2022 Labeler - WAL-MART STORES INC (051957769)