NDC | 49973-667-20, 49973-667-60 |
Set ID | 22845cac-8011-4ea8-b35e-b72973eddb44 |
Category | HUMAN OTC DRUG LABEL |
Packager | i-Health, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Warnings:
For oral use only. This product will not cure a yeast infection.
Do not use if you have never had a vaginal yeast infection diagnosed by a doctor.
Ask a doctor before use if you
- have vaginal itching and discomfort for the first time.
- have abdominal pain, fever, chills, nausea, vomiting, or foul-smelling vaginal discharge. You may have a serious condition.
- get vaginal yeast infections often (such as once a month or three in six months).
- may have been exposed to human immunodeficiency virus (HIV) that causes AIDS.
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- GENERAL PRECAUTIONS
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AZO YEAST PLUS
candida albicans, wood creosote, sodium chloride, and sulfur tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49973-667 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 CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) MAGNESIUM STEARATE (UNII: 70097M6I30) HYPROMELLOSES (UNII: 3NXW29V3WO) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) Product Characteristics Color white Score no score Shape ROUND Size 10mm Flavor Imprint Code A Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49973-667-60 60 in 1 BOX 04/01/2014 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:49973-667-20 20 in 1 BOX 04/25/2018 2 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 01/01/2014 Labeler - i-Health, Inc. (061427694)