Steritouch Hand Sanitizer

Manufacturer
GUANGZHOU NODA PHARMACEUTICAL TECHNOLOGY INCORPORATED CO., LTD
Effective date
2022-01-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:19:19

Label at a glance#

ProductSteritouch Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Wet hands thoroughly with products Briskly rub hands together until dry Supervise use with children under 10 years of age

Storage and handling

Store in a cool, dry place between 68°F-77°F

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

The hand sanitizer contains:

  1. Alcohol (ethanol) (70%, volume/volume (v/v))
  2. GLYCERIN (2% v/v).
  3. CARBOMER COPOLYMER TYPE A (0.4% v/v).
  4. Sterile distilled water or boiled cold water.
  5. TROLAMINE(0.4% v/v)
  6. PROPYLENE GLYCOL (0.5% v/v)
  7. ALOE VERA LEAF(2% v/v)
  8. .ALPHA.-TOCOPHEROL ACETATE (0.5% v/v)

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame. May discolor certain fabrics.

Do not use

OTC - DO NOT USE SECTION

  • 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.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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

  • Wet hands thoroughly with products
  • Briskly rub hands together until dry
  • Supervise use with children under 10 years of age

Other information

STORAGE AND HANDLING SECTION

Store in a cool, dry place between 68°F-77°F

Inactive ingredients

INACTIVE INGREDIENT SECTION

GLYCERIN,CARBOMER COPOLYMER TYPE A,PURIFIED WATER,TROLAMINE,PROPYLENE GLYCOL,ALOE VERA LEAF,

.ALPHA.-TOCOPHEROL ACETATE (0.5% v/v)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

​480 mL NDC: 78098-001-01 480ml label 1480ml label 1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78098-00178098-001-01

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 · Source PDF

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
0e7aeb3b-385f-1ee3-e063-6394a90a9d2fa5f96a02-2602-10e8-e053-2995a90afe4a2024-01-08WarningsExact identifier
spl set id: a5f96a02-2602-10e8-e053-2995a90afe4a

Reported adverse events (FAERS/openFDA)#

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