Anti-Itch Wipes

Manufacturer
Diamond Wipes International
Effective date
2023-12-07
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:18:10

Label at a glance#

ProductAnti-Itch Wipes
Active ingredientPRAMOXINE HYDROCHLORIDE
Label structure12 sections

Indications and uses

For the temporary relief of pain and itching associated with minor skin irritations

Dosage and administration

Adults and children 12 years of age and older: • Apply to affected area not more than 3 or 4 times daily. Children under 12 years of age: Consult a doctor

Storage and handling

Store at a controlled room temperature 77°F (20-25°C)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Pramoxine Hydrochloride 1%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of pain and itching associated with minor skin irritations

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes.

Stop use and ask doctor if:

OTC - DO NOT USE SECTION

• Condition worsens

• If symptoms persist for more than 7 days, or clear up and reoccur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions:

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older: • Apply to affected area not more than 3 or 4 times daily.

Children under 12 years of age: Consult a doctor

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Aloe Barbadensis Leaf Extract, *Aloe Barbadensis Leaf Juice, Althaea officinalis Root Extract, Avena Sativa (Oat) Kernel Extract, Calendula Officinalis Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Citric Acid, Cocamidopropyl PG-Dimonium Chloride Phosphate, Cocos Nucifera (Coconut) Fruit Extract, Cucumis Sativus (Cucumber) Fruit

Extract, Disodium Cocoamphodiacetate, Ethylhexylglycerin, Euterpe Oleracea Fruit Extract, Fragrance, Glycerin, Hamamelis Virginiana (Witch Hazel) Water, Helianthus Annuus (Sunflower) Seed Oil, *Honey, Lactobacillus, Lactobacillus Ferment, Lavandula Angustifolia (Lavender) Oil, Phenoxyethanol, Polyglyceryl-4 Caprate, Punica Granatum Fruit Extract, Rosa Centifolia Flower Water, Sodium Chloride, Tetrasodium Glutamate Diacetate Tocopheryl Acetate, *Apple Cider Vinegar, Water

*Organic Ingredients

Other Information:

STORAGE AND HANDLING SECTION

Store at a controlled room temperature 77°F (20-25°C)

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MAXIMUM STRENGTH

the Honey Pot ® company

PLANT-DERIVED FEMININE CARE™

RELIEF

ANTI ITCH

soothing wipes

1% PRAMOXINE HYDROCHLORIDE

(EXTERNAL ANALGESIC)

for temporary relief of itching and discomfort

30 COUNT

9363.1

POWERED BY HERBS™

FIND US ONLINE:

THEHONEYPOT.CO

@THEHONEYPOTCO

DISTRIBUTED BY THE HONEY POT CO.
P.O. BOX 93326 ATLANTA, GA 30377
THEHONEYPOT.CO

MADE IN USA WITH GLOBAL COMPONENTS

8 50021 58936 3

9363.1

TAMPER EVIDENT UNIT, DO NOT USE IF PERFORATED FLAP HAS BEEN OPENED, IS MISSING OR INCOMPLETELY SEALEDS

MADE WITH WITCH HAZEL

ALOE

CALENDULA

LAVENDER

THE FUTURE OF
PERSONAL WELLNESS™

MADE BY HUMANS WITH VAGINAS, FOR HUMANS WITH VAGINAS ®

We’re formulating a more transparent world rooted in holistic solutions for total wellness. A world where the power of herbs meets the efficacy of science and inspires accessible self-care rituals for intimate health. Clinically-tested formulas and plant-derived ingredients designed to give you a good day and even better tomorrow.

THE HONEY POT’S FIRST TREATMENT LINE DESIGNED TO RELIEVE ITCH.

TRY THEM ALL:

♦ ANTI-ITCH SOOTHING SPRAY
♦ ANTI-ITCH VULVA CREAM
♦ SOOTHING WASH*

*when used as a regimen with anti-itch wipes, cream or spray.

Drug Facts

Active Ingredient: Pramoxine Hydrochloride 1%
Purpose: External Analgesic

Uses: For the temporary relief of pain and itching associated with minor skin irritations

Warnings:
For external use only

When using this product: avoid contact with eyes.
Stop use and ask doctor if:
• Condition worsens
• If symptoms persist for more than 7 days, or clear up and reoccur again within a few days
Keep out of reach of of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions: Adults and children 12 years of age and older: • Apply to affected area not more than 3 or 4 times daily.

Children under 12 years of age: Consult a doctor

Inactive Ingredients: Aloe Barbadensis Leaf Extract, *Aloe Barbadensis Leaf Juice, Althaea officinalis Root Extract, Avena Sativa (Oat) Kernel Extract, Calendula Officinalis Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Citric Acid, Cocamidopropyl PG-Dimonium Chloride Phosphate, Cocos Nucifera (Coconut) Fruit Extract, Cucumis Sativus (Cucumber) Fruit
Extract, Disodium Cocoamphodiacetate, Ethylhexylglycerin, Euterpe Oleracea Fruit Extract, Fragrance, Glycerin, Hamamelis Virginiana (Witch Hazel) Water, Helianthus Annuus (Sunflower) Seed Oil, *Honey, Lactobacillus, Lactobacillus Ferment, Lavandula Angustifolia (Lavender) Oil, Phenoxyethanol, Polyglyceryl-4 Caprate, Punica Granatum Fruit Extract, Rosa Centifolia Flower Water, Sodium Chloride, Tetrasodium Glutamate Diacetate Tocopheryl Acetate, *Apple Cider Vinegar, Water
*Organic Ingredients

Other Information: Store at a controlled room temperature 77°F (20-25°C).

Questions: For questions and general information visit us at www.thehoneypot.co/contact

the Honey Pot ® company

DESIGNED TO RELIEVE ITCH

CALENDULA ALOE LAVENDER

RELIEF

powered by herbs ®

8 50021 58936 3

RELIEF

LABELLABEL

LABELLABEL

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64709-15864709-158-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

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
0bef2d6f-3368-e653-e063-6394a90a5aefe2c3d9d3-6f30-8edb-e053-2995a90a0eff2023-12-07WarningsExact identifier
spl id: 0bef2d6f-3368-e653-e063-6394a90a5aef
spl set id: e2c3d9d3-6f30-8edb-e053-2995a90a0eff

Reported adverse events (FAERS/openFDA)#

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