HES CLEAN FOR WOMAN

Manufacturer
DOCTOR C&C
Effective date
2014-12-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:40:59

Label at a glance#

ProductHES CLEAN FOR WOMAN
Active ingredientAlcohol
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Alcohol 1%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: Aqua (Hydrogen Ionized Water), Rosa Centifolia Flower Water, Butylene Glycol, Witch Hazel Extract, Lavender Flower/Leaf/Stem Extract, Basil Flower/Leaf Extract, Marshmallow Leaf/Root Extract, Heartleaf Houttuynia Extract, Chamomile Flower Extract, Rosemary Extract, Fennel Leaf Extract, Apple Water, Decyl Glucoside, Indian Lettuce Extract, Corydalis ochotensis Turcz Extract, Whitlow Grass Extract, Goosefoot Flower Extract, Sarcodon Aspratus Extract, Maka Root Extract, Pomegranate Extract, Fig Extract, Mulberry Extract, Ginkgo Extract, Hydroxyethylcellulose, Arginine, 1,2-Hexandiol, Ethanol, Lactic Acid, Soy Isoflavones, Black Cohosh Extracts, Knotweed Root Extract, Kudzu Root Extract, Cnidium Officinale Root Extract, Punica Granatum Extract, Red Clover Flower Extract, Thai Kudzu Root Extract, PEG-40 Hydrogenated Castor Oil, Soapberry Extract, Human Oligopeptide-1, Ascorbic Acid, Pyridoxine HCl, Menthol, Damask Rose Oil

PURPOSE

OTC - PURPOSE SECTION

Purpose: Antifungal

WARNINGS

WARNINGS SECTION

Warnings:
1. Please discontinue use immediately in the event that you experience any of the following side effects from using this product, and consult a dermatologist as the symptoms may get worse with continued use.

(a) Adverse skin reactions occur upon its application which may involve red spots, swelling, itchiness, and other skin irritation.
(b) The applied part shows signs of any of the symptoms mentioned above after exposure to the direct sunlight.

2. Do not apply to wounds and the area affected by dermatitis, eczema, and other irritations.

3. Precautions for handling and storage
(a) Always close the cap after each use.
(b) Always keep the product out of the reach of infants.
(c) Do not store the product in high and low temperatures. It should also be kept out of direct sunlight.

4. Vulvar Cleanser
(a) It should only be used on the vulva.
(b) It should not be used for long periods of time.
(c) It should be used with extreme caution when there are affected areas on the (vulvar) skin or the surrounding area has become contaminated.
(d) It should not be used on children under 3 years of age.
(e) It is not recommended for use during pregnancy and it is advised that you discontinue its use on the vulva until you deliver a baby as it may get into the eyes of the newborn baby.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN:
Keep this product out of reach of infants and young children.

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & usage:
Wet your vulva thoroughly with running water (preferably mild in temperature). Apply a suitable amount (2-3g) evenly to the region and massage gently. Rinse thoroughly in clean, lukewarm water.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: 2-3g per use

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42979-140-012020-01-31C16284748780-19d75b9d0-39cd-f424-e053-dadaa90a57ceb87942d3-9f48-4d15-a8ad-d53e8f1af7f2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42979-140-01HES CLEAN FOR WOMAN180 mL in 1 CARTONSOLUTION1801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42979-140HES CLEAN FOR WOMAN (ALCOHOL) SOLUTION [DOCTOR C&C]1Legacy NDC, 1 package rows20141203_b87942d3-9f48-4d15-a8ad-d53e8f1af7f2.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AlcoholACTIVE INGREDIENT3K9958V90M1
ALCOHOLACTIVE MOIETY3K9958V90M1
Butylene GlycolINACTIVE INGREDIENT3XUS85K0RA1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42979-14042979-140-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
Alcohol3K9958V90MACTIB
WATER059QF0KO0RIACT
Butylene Glycol3XUS85K0RAIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
a56416f5-5645-40ba-b437-9c4c90760706b87942d3-9f48-4d15-a8ad-d53e8f1af7f22014-12-03WarningsExact identifier
spl id: a56416f5-5645-40ba-b437-9c4c90760706
spl set id: b87942d3-9f48-4d15-a8ad-d53e8f1af7f2

Reported adverse events (FAERS/openFDA)#

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