24909-211 - Femmesil Cleasing Bar

Manufacturer
Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions, LLC
Effective date
2026-06-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-07-17 21:34:13

Label at a glance#

ProductFemmesil Cleansing Bar
Active ingredientTHUJA OCCIDENTALIS LEAF
Label structure8 sections

Indications and uses

Helps relieve vaginal yeast infection symptoms.

Dosage and administration

Children under 12: Ask a physician. Adults and children 12 years and over: Cleansing bar may be used outside the vaginal area daily, as needed. For best results, use in conjunction with Femmesil Cream or Ultra Therapy Ointment. Store at room temperature.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Thuja Occidentalis 6X HPUS

Purpose

OTC - PURPOSE SECTION

Antifungal

The letters HPUS indicate the component in this product is officially monographed in the Homeopathic Pharmacopeia of the United States

Uses

INDICATIONS & USAGE SECTION

Helps relieve vaginal yeast infection symptoms.

Warnings

WARNINGS SECTION

For external vaginal use only. Do not use if you have never had a vaginal yeast infection diagnosed by a doctor; if you have a fever (higher than 100° F), pain in the lower abdomen, back, or either shoulder, or a foul-smelling vaginal discharge. You should see a doctor for treatment of these symptoms.

Stop use and ask a doctor if symptoms do not get better in 3 days or last more than 7 days.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Children under 12: Ask a physician. Adults and children 12 years and over: Cleansing bar may be used outside the vaginal area daily, as needed. For best results, use in conjunction with Femmesil Cream or Ultra Therapy Ointment. Store at room temperature.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

beeswax, citric acid, coconut oil, glycerin, jojoba oil, lavender oil, magnesium oxide, peppermint oil, propylene glycol, silver
stearate, sodium chloride, sodium citrate, sodium laurate, sodium laureth sulfate, sodium lauryl sulfate, sodium myristate, sodium oleate, sodium olivate, sodium shea butterate, sodium stearate, sorbitol, tea tree oil, tetrasodium etidronate, tetrasodium iminodisuccinate, titanium dioxide, water, zinc oxide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

femmisil Cleansing Barfemmisil Cleansing Bar

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24909-21124909-211-75, 24909-211-85

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12022-05-25full-release2026-06-01 02:17:40

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
Femmesil Cleansing BarTHUJA OCCIDENTALISAidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions, LLCc29135e0-4be7-4bed-bb3e-b9cbe10e5a732026-06-25WarningsExact identifier
ndc (package): 24909-211-75
ndc (package): 24909-211-85
ndc (product): 24909-211
ndc11 (package): 24909021175
ndc11 (package): 24909021185
spl id: 55142281-4836-6819-e063-6394a90a158f
spl set id: c29135e0-4be7-4bed-bb3e-b9cbe10e5a73

Reported adverse events (FAERS/openFDA)#

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