Label: THE ERASER- sodium borate, collinsonia canadensis root, berberis vulgaris root bark, and hamamelis virginiana root bark/stem bark suppository
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Contains inactivated NDC Code(s)
NDC Code(s): 72764-003-01 - Packager: Brandable
- Category: HUMAN OTC DRUG LABEL
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 November 18, 2019
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Uses
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Warnings
For vaginal use only. Use only as directed.
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 more 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 your 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
When using this product
- If you do not get complete relief ask a doctor before using another product.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 14 Vaginal Suppositories Carton
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INGREDIENTS AND APPEARANCE
THE ERASER
sodium borate, collinsonia canadensis root, berberis vulgaris root bark, and hamamelis virginiana root bark/stem bark suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72764-003 Route of Administration VAGINAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 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] Berberis Vulgaris Root Bark (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) Berberis Vulgaris Root Bark 6 [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 BACILLUS COAGULANS (UNII: ISK1LOY57E) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) POLYETHYLENE GLYCOL 1450 (UNII: OJ4Z5Z32L4) Product Characteristics Color WHITE Score Shape OVAL Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72764-003-01 1 in 1 CARTON 02/28/2019 1 14 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 02/28/2019 Labeler - Brandable (080414109)