FDA.reportPublic FDA data

PALMA HAND SANITIZER

Manufacturer
UNITRADE FZE
Effective date
2024-12-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:47:32

Label at a glance#

ProductPALMA HAND SANITIZER
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

• hand sanitizer to decrease bacteria on the skin  • recommended for repeated use  • for use when soap and water are not available

Dosage and administration

• wet hands thoroughly with product and allow to dry without wiping • supervise children under 6 years of age when using this product to avoid swallowing

Storage and handling

• store between 15-30°C (59-86°F) • avoid freezing and excessive heat above 40°C (104°F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses 

INDICATIONS & USAGE SECTION

• hand sanitizer to decrease bacteria on the skin  • recommended for repeated use  • for use when soap and water are not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame
For external use only

Do not use  • in children less than 2 months of age  • on open skin wounds

When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if  • irritation and redness develop  • condition persists for more than 72 hours

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

• wet hands thoroughly with product and allow to dry without wiping • supervise children under 6 years of age when using this product to avoid swallowing

Other information

STORAGE AND HANDLING SECTION

• store between 15-30°C (59-86°F) • avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, caprylic /capric triglyceride, avocado (Persea gratissima) oil, propylene glycol, glycerin, jojoba (Simmondsia chinensis) seed oil, peg-40 hydrogenated castor oil, polyacrylamide, c13-14 isoparaffin, laureth-7, acrylates / c10-30 alkyl acrylates crosspolymer, niacinamide, sodium hyaluronate, tocopheryl acetate, panthenol, gotu kola (Centella asiatica) root extract, triethanolamine, fragrance.

Questions? 1-516-535-5555

OTC - QUESTIONS SECTION

You may also report serious side effects to this phone number. Mon-Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

MOISTURIZING

WITH AVOCADO OIL, JOJOBA OIL, VITAMIN B3 & B5

PROTECT. HYDRATE. NOURISH.

Distributed by:
Palma De Salus, Inc
320 Country Road, Suite 205
Garden City, NY 11530, U.S.A


Made in U.A.E.
Designed in Los Angeles
palmadesalus.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN3
581662ethanol 0.7 ML/ML Topical GelSCD3
581662ethanol 70 % Topical GelSY3
581662ethyl alcohol 70 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81286-101-102022-11-16C16284748780-1e4f33bdf-a8b7-d8a0-e053-dadaa90a6e4ePALMA DE SALUS HAND SANITIZER
81286-101-102022-07-29C16284748780-1e4f33bdf-a8b7-d8a0-e053-dadaa90a6e4ePALMA DE SALUS HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81286-101-10PALMA HAND SANITIZER325 mL in 1 BOTTLE, PUMPGEL3253
81286-101-10PALMA HAND SANITIZER1 in 1 CARTONGEL13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81286-101PALMA HAND SANITIZER (ETHYL ALCOHOL) GEL [UNITRADE FZE]3Legacy NDC, 2 package rows20241222_6d35fbce-e9ae-45df-84ef-43188a0f4230.zip

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
81286-10181286-101-10

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
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
AVOCADO OIL6VNO72PFC1IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
JOJOBA OIL724GKU717MIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
POLYACRYLAMIDE (1300000 MW)SC5Y4X78TGIACT
C13-14 ISOPARAFFINE4F12ROE70IACT
LAURETH-7Z95S6G8201IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
NIACINAMIDE25X51I8RD4IACT
HYALURONATE SODIUMYSE9PPT4THIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
PANTHENOLWV9CM0O67ZIACT
CENTELLA ASIATICA LEAF6810070TYDIACT
TROLAMINE9O3K93S3TKIACT

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
520e9957-f66f-4969-84dc-287aff057aaf6d35fbce-e9ae-45df-84ef-43188a0f42302024-12-19WarningsExact identifier
spl id: 520e9957-f66f-4969-84dc-287aff057aaf
spl set id: 6d35fbce-e9ae-45df-84ef-43188a0f4230

Reported adverse events (FAERS/openFDA)#

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