FDA.reportPublic FDA data

Puriton SKIN PROTECTANT HOMEOPATHIC

Manufacturer
Kadesh, Inc.
Effective date
2016-08-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:11

Label at a glance#

ProductPuriton SKIN PROTECTANT HOMEOPATHIC
Active ingredientALUMINUM OXIDE, CALCIUM FLUORIDE, CALCIUM SILICATE, MAGNESIUM SULFATE HEPTAHYDRATE, SILICON DIOXIDE, SULFUR, TITANIUM, ZINC
Label structure11 sections

Indications and uses

• Temporarily protects and helps to relieve minor skin irritation   • rashes  • eczema • Temporarily protects minor • scratches • burns     • chapped or cracked skin

Dosage and administration

• Spray as needed to affected areas, both face and body. • Children under two years old, ask a doctor.

Storage and handling

• Store at room temperature. • Tamper Evident: Do not use if neckband on bottle is broken or missing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alumina 7X HPUS
Calcarea Fluorica 6X HPUS
Calcarea Silicata 5X HPUS
Magnesia Sulphurica 7X HPUS
Silicea 4X HPUS
Sulphur 4X HPUS
Titanium Metallicum 7X HPUS
Zincum Metallicum 8X HPUS

The letters HPUS indicate that this ingredients is officially included in the Homoeopathic pharmacopoeia of the United States.

Purpose

OTC - PURPOSE SECTION

Dry, Itchy skin
Chaps, Cracks
Itchy Skin
Itchy Skin
Out-breaks on skin
Itchy skin, Eczema
Eczema
Eczema

Uses

INDICATIONS & USAGE SECTION

• Temporarily protects and helps to relieve minor skin irritation

  • rashes  • eczema
• Temporarily protects minor • scratches • burns  

  • chapped or cracked skin

Warnings

WARNINGS SECTION

Do not Use  • on broken skin  • large areas of the skin

When using this product

  • do not get into eyes  • replace cap after using

  • Use on mild to moderate eczema

Stop use and ask a doctor if  • condition worsens  • condition last more than 7 days or clear up and occur again within a few days

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.

Directions

DOSAGE & ADMINISTRATION SECTION

• Spray as needed to affected areas, both face and body.
• Children under two years old, ask a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alumina Silicata, Cerium Oxalicum, Ferrum Metallicum, Ferrum Muriaticum, Ferrum Phosphoricum, Kali Silicatum, Magnesia Muriatica, Natrum Muriaticum, Natrum Nitricum, Phosphorous, Distilled Water

Other information

STORAGE AND HANDLING SECTION

• Store at room temperature.
• Tamper Evident: Do not use if neckband on bottle is broken or missing.

OTC - QUESTIONS SECTION

Questions or Comments? 1-844-KADESH1
Mon - Fri. 9.00 a.m. - 6.00 p.m. PST
www.puriton.us

SPL UNCLASSIFIED SECTION

treats​ dry, itchy skin

gentle, skin moisturizer

relieves breakouts and cracked skin

helps minor cuts and burns

100% Pure & Natural
100% Preservative-Free

Made in the U.S.A

Distributed by:
U.S. Continental

Corona, CA 92879
 info@kadesh99.com

Packaging​

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70796-002-042020-01-31C16284748780-19d75b9d0-4c81-f424-e053-dadaa90a57cepuriton SKIN PROTECTANT HOMEOPATHIC

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70796-002-04Puriton SKIN PROTECTANT HOMEOPATHIC118 mL in 1 BOTTLE, SPRAYSPRAY1181
70796-002-04Puriton SKIN PROTECTANT HOMEOPATHIC1 in 1 CARTONSPRAY11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70796-002PURITON SKIN PROTECTANT HOMEOPATHIC (ALUMINA, CALCAREA FLUORICA, CALCAREA SILICATA, MAGNESIA SULPHURICA, SILICEA, SULPHUR, TITANIUM METALLICUM, ZINCUM METALLICUM) SPRAY [KADESH, INC.]1Legacy NDC, 2 package rows20161001_3c9fdbb9-2c98-47d8-9a69-470affce4b01.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70796-00270796-002-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM OXIDELMI26O6933ACTIB
CALCIUM FLUORIDEO3B55K4YKIACTIB
CALCIUM SILICATES4255P4G5MACTIB
MAGNESIUM SULFATE HEPTAHYDRATESK47B8698TACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
SULFUR70FD1KFU70ACTIB
TITANIUMD1JT611TNEACTIB
ZINCJ41CSQ7QDSACTIB
KAOLIN24H4NWX5COIACT
CEROUS OXALATE NONAHYDRATE0UV74P3R0JIACT
IRONE1UOL152H7IACT
FERRIC CHLORIDE HEXAHYDRATE0I2XIN602UIACT
FERROSOFERRIC PHOSPHATE91GQH8I5F7IACT
POTASSIUM SILICATEJ86L1GUL6KIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM NITRATE8M4L3H2ZVZIACT
PHOSPHORUS27YLU75U4WIACT
WATER059QF0KO0RIACT

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
3b4a8763-1e6e-4f62-8bde-851478f268563c9fdbb9-2c98-47d8-9a69-470affce4b012016-08-06WarningsExact identifier
spl id: 3b4a8763-1e6e-4f62-8bde-851478f26856
spl set id: 3c9fdbb9-2c98-47d8-9a69-470affce4b01

Reported adverse events (FAERS/openFDA)#

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