NEEM HAND SANITIZER

Manufacturer
Maharishi Ayur-Ved Products International Corporation | Royal Labs Natural Cosmetics, Inc.
Effective date
2023-01-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:40:40

Label at a glance#

ProductNEEM HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Ethyl Alcohol 62% v/v.

OTC - PURPOSE SECTION

Purpose Antiseptic

INDICATIONS & USAGE SECTION

Uses: Hand sanitizer to help reduce germs that potentially can cause disease. Recommended for repeated use.

WARNINGS SECTION

Warnings For external use only. Flammable. Keep away from fire or flame.

OTC - DO NOT USE SECTION

Do not use in children less than 2 months of age. On open skin 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 - ASK DOCTOR SECTION

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

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.

DOSAGE & ADMINISTRATION SECTION

Directions Spray enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 to avoid swallowing.

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Aqua (purified water), Organic glycerin (vegetable), Aloe barbadensis (aloe vera) leaf juice, Herb blend [Curcuma zedoaria (white turmeric) rhizome extract, Azadirachta indica (neem) leaf extract], Menthol, Mentha piperita (peppermint) oil.

NEEM HAND SANITIZER

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2oz label2oz labelNDC 81587-622-02

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81587-62281587-622-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
f2146723-ee50-1753-e053-2995a90ac5b9c3cf3c8b-44fe-899e-e053-2995a90aa60e2023-01-12WarningsExact identifier
spl id: f2146723-ee50-1753-e053-2995a90ac5b9
spl set id: c3cf3c8b-44fe-899e-e053-2995a90aa60e

Reported adverse events (FAERS/openFDA)#

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