FDA.reportPublic FDA data

AHAVA Moisturizing Hand Sanitizing Foam

Manufacturer
AHAVA Dead Sea Laboratories Ltd
Effective date
2020-06-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:24:34

Label at a glance#

ProductAHAVA Moisturizing Hand Sanitizing Foam
Active ingredientBenzalkonium Chloride
Label structure11 sections

Indications and uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. Quick and effective cleaning when soap and water are not available.

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. Quick and effective cleaning when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

  • In children less than 2 months age
  • On open wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Mineral Spring Water), Glycerin, PEG-6 Caprylic/Capric glycerides, PVP, Phenoxyethanol, Parfum (Fragrance), Hexyl Cinnamal, Limonene, Geraniol, Linalool, Citronellol, Chlorphenesin, Caprylyl Glycol, Didecyldimonium Chloride, Sodium Benzoate, Potassium Sorbate, Aloe Barbadensis (Aloe-Vera) Leaf Juice, Panthenol (Pro Vitamin B5), Maris Aqua (Dead Sea Water/Osmoter).

Questions or comments

OTC - QUESTIONS SECTION

Call toll free 1-800-366-7254

SPL UNCLASSIFIED SECTION

Manufactured by AHAVA Dead Sea Laboratories Ltd. Dead Sea, Israel, 8698000.

Distributed by:
In EU: AHAVA Cosmetics GmbH, Borsigstr. 36, D-65205 Wiesbaden, Germany
In US: AHAVA N.A. LLC, New York, NY 10001

PRINCIPAL DISPLAY PANEL - 200 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AHAVA

MOISTURIZING
HAND SANITIZING FOAM

Rinse free • Alcohol free

BODY CLEANSING & RENEWAL

PRINCIPAL DISPLAY PANEL - 200 mL Bottle Label
PRINCIPAL DISPLAY PANEL - 200 mL Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60289-294-312023-11-15C16284748780-1f386c64a-39d0-0266-e053-dadaa90a7c1aAHAVA Moisturizing Hand Sanitizing Foam
60289-294-312023-01-30C16284748780-1f386c64a-39d0-0266-e053-dadaa90a7c1aAHAVA Moisturizing Hand Sanitizing Foam

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60289-29460289-294-31

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
Benzalkonium ChlorideF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CAPRYLOCAPROYL POLYOXYLGLYCERIDES 6GO50W2HWO8IACT
POVIDONE, UNSPECIFIEDFZ989GH94EIACT
PHENOXYETHANOLHIE492ZZ3TIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
LIMONENE, (+)-GFD7C86Q1WIACT
GERANIOLL837108USYIACT
LINALOOL, (+/-)-D81QY6I88EIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
CHLORPHENESINI670DAL4SZIACT
CAPRYLYL GLYCOL00YIU5438UIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
SODIUM BENZOATEOJ245FE5EUIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
ALOE VERA LEAFZY81Z83H0XIACT
DEXPANTHENOL1O6C93RI7ZIACT

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
c14b4cc3-3675-4d57-8f86-27fb30955e78ef3bd935-9503-4303-8b57-56ef40e0fb502023-11-07WarningsExact identifier
spl set id: ef3bd935-9503-4303-8b57-56ef40e0fb50

Reported adverse events (FAERS/openFDA)#

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