FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
Maapilim Usa, Inc.
Effective date
2022-02-07
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:09:24

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

APPLY A SUFFICIENT AMOUNT OF PRODUCT TO YOUR PALM TO COVER BOTH HANDS. RUB UNTIL DRY.

Storage and handling

STORE BELOW 110F (43C)

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 70% V/V

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USE

INDICATIONS & USAGE SECTION

TO DECREASE BACTERIA ON THE SKIN THAT POTENTIALLY CAN CAUSE DISEASE

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

FLAMMABLE, KEEP AWAY FROM HEAT OR FLAME.

DO NOT USE IN THE EYES.

STOP USE AND ASK A DOCTOR IF IRRITATION OR PAIN OCCURS.

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

  • APPLY A SUFFICIENT AMOUNT OF PRODUCT TO YOUR PALM TO COVER BOTH HANDS.
  • RUB UNTIL DRY.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

STORE BELOW 110F (43C)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

AQUA, ALOE BARBADENSIS LEAF JUICE, GLYCERIN, HYDROXYETHYLCELLULOSE, FRAGRANCE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Maapilim_Hand Sanitizer01b LBL_Maapilim_Hand Sanitizer

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77239-101-112022-02-07C16284748780-1d6a99b39-3fa2-a426-e053-dadaa90af4c2MAAPILM - HAND SANITIZER (77239-101)
77239-101-112022-01-28C16284748780-1d6a99b39-3fa2-a426-e053-dadaa90af4c2MAAPILM - HAND SANITIZER (77239-101)

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77239-10177239-101-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)R33S7TK2EPIACT
ALCOHOL3K9958V90MACTIB

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
d772cf43-d253-7043-e053-2a95a90a9eb3a3b048d3-3eea-4014-905d-1a0f017985a72022-02-07WarningsExact identifier
spl id: d772cf43-d253-7043-e053-2a95a90a9eb3
spl set id: a3b048d3-3eea-4014-905d-1a0f017985a7

Reported adverse events (FAERS/openFDA)#

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