Hand Sanitizer

Manufacturer
Raining Rose | Aire-Master America, Inc
Effective date
2021-05-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:40:14

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

WARNINGS SECTION

Flammable. Keep away from fire and flame. For external use only. Do not use in the eyes. In case of contact, rinse eyes thoroughly with water. Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Glycerin, Fragrance, Aloe Barbadensis Leaf Juice, Essential Oil.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

C10876C10876

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65692-2068-12023-01-30C16284748780-1f386c649-a200-0266-e053-dadaa90a7c1ac1af64d5-ef8c-fd7b-e053-2a95a90aea93

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65692-2068-1Hand Sanitizer10 mL in 1 BOTTLE, SPRAYLIQUID101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65692-2068HAND SANITIZER LIQUID [RAINING ROSE]1Legacy NDC, 1 package rows20210508_c1af64d5-ef8c-fd7b-e053-2a95a90aea93.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65692-206865692-2068-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
c1af64d5-ef8d-fd7b-e053-2a95a90aea93c1af64d5-ef8c-fd7b-e053-2a95a90aea932021-05-06WarningsExact identifier
spl id: c1af64d5-ef8d-fd7b-e053-2a95a90aea93
spl set id: c1af64d5-ef8c-fd7b-e053-2a95a90aea93

Reported adverse events (FAERS/openFDA)#

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