FDA.reportPublic FDA data

The Eraser

Manufacturer
Brandable
Effective date
2019-11-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:11:34

Label at a glance#

ProductThe Eraser
Active ingredientSodium Borate, Collinsonia Canadensis Root, Berberis Vulgaris Root Bark, Hamamelis Virginiana Root Bark/Stem Bark
Label structure11 sections

Indications and uses

For the temporary relief of symptoms associated with vaginal yeast infection, including: † itching burning irritation

Dosage and administration

Remove one suppository from the foil wrap and place in the applicator. Insert suppository into the vagina with the applicator. Remove applicator and cleanse thoroughly with soap and water. Use one suppository daily for seven days.

Storage and handling

Suppositories are not a contraceptive and should not be used to prevent pregnancy. Do not Use if foil seal on suppositories is torn, open or incompletely sealed Purchase if carton is open Store at room temperature Lot number and expiration dates: see bottom of box

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Borax 3X* HPUS** (Sodium Borate)
Collinsonia Canadensis 3X* HPUS** (Stone Root)
Berberis Vulgaris 6X* HPUS** (Barberry)
Hamamelis Virginiana 6X* HPUS** (Witch Hazel)

Purpose

OTC - PURPOSE SECTION

Temporary relief from symptoms of vaginal yeast infections†

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of symptoms associated with vaginal yeast infection, including:†

  • itching
  • burning
  • irritation

Warnings

WARNINGS SECTION

For vaginal use only. Use only as directed.

OTC - DO NOT USE SECTION

Do not use if you have never had a vaginal yeast infection diagnosed by a doctor.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • 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

OTC - WHEN USING SECTION

  • If you do not get complete relief ask a doctor before using another product.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Symptoms last more than 7 days
  • You get a rash or hives, abdominal pain, fever, chills, nausea, vomiting, or foul-smelling vaginal discharge.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Remove one suppository from the foil wrap and place in the applicator. Insert suppository into the vagina with the applicator. Remove applicator and cleanse thoroughly with soap and water. Use one suppository daily for seven days.

Other information

STORAGE AND HANDLING SECTION

  • Suppositories are not a contraceptive and should not be used to prevent pregnancy.
  • Do not
    • Use if foil seal on suppositories is torn, open or incompletely sealed
    • Purchase if carton is open
  • Store at room temperature
  • Lot number and expiration dates: see bottom of box

Inactive ingredients

INACTIVE INGREDIENT SECTION

Bacillus coagulans (Lactospore®), Polyethylene Glycols

Questions or comments?

OTC - QUESTIONS SECTION

(877) 281-3001

SPL UNCLASSIFIED SECTION

Distributed by Brandable, Inc.
DBA Queen V®
269 S. Beverly Drive, Suite 8
Beverly Hills, CA 90212

PRINCIPAL DISPLAY PANEL - 14 Vaginal Suppositories Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

YEAST INFECTION RELIEF

QUEEN V®

the eraser

homeopathic formula

helps treat symptoms of
vaginal yeast infections

A homeopathic approach to help
relieve painful symptoms of
yeast infections in your Queen V.†

14 Vaginal
Suppositories

Reusable Applicator Included

PRINCIPAL DISPLAY PANEL - 14 Vaginal Suppositories Carton
PRINCIPAL DISPLAY PANEL - 14 Vaginal Suppositories Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72764-003-012021-01-29C16284748780-1ba0f9c33-5ca6-a910-e053-dadaa90a0b85The Eraser

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72764-003-01The Eraser1 in 1 CARTONSUPPOSITORY11
72764-003-01The Eraser14 in 1 PACKETSUPPOSITORY141

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72764-003THE ERASER (SODIUM BORATE, COLLINSONIA CANADENSIS ROOT, BERBERIS VULGARIS ROOT BARK, AND HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK) SUPPOSITORY [BRANDABLE]1Legacy NDC, 2 package rows20191120_ef41d72c-2c0e-4382-b617-b15ddf4f30b7.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72764-00372764-003-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
Sodium Borate91MBZ8H3QOACTIB
Collinsonia Canadensis RootO2630F3XDRACTIB
Berberis Vulgaris Root Bark1TH8Q20J0UACTIB
Hamamelis Virginiana Root Bark/Stem BarkT7S323PKJSACTIB
BACILLUS COAGULANSISK1LOY57EIACT
POLYETHYLENE GLYCOL 400B697894SGQIACT
POLYETHYLENE GLYCOL 1450OJ4Z5Z32L4IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ad772470-cd29-42eb-a9d9-91004fae526bef41d72c-2c0e-4382-b617-b15ddf4f30b72019-11-18WarningsExact identifier
spl id: ad772470-cd29-42eb-a9d9-91004fae526b
spl set id: ef41d72c-2c0e-4382-b617-b15ddf4f30b7

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.