White Rose Liquid Hand Sanitizer

Manufacturer
J. Strickland and Co.
Effective date
2020-03-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:38:18

Label at a glance#

ProductWhite Rose Liquid Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Place enough product on hands to cover all surfaces.  Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

​Active ingredient[s]

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v

​Purpose

OTC - PURPOSE SECTION

Antiseptic

​Use[s]:

INDICATIONS & USAGE SECTION

Hand sanitizer to help decrease bacteria that can cause disease.  For use when soap and water are not available.

​Warnings:

WARNINGS SECTION

For external use only. Flammable.  Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

When using this product

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

irritation or rash occurs.  These may be signs of serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

​Directions:

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces.  Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

​Other information:

SPL UNCLASSIFIED SECTION

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

​Inactie Ingredients:

INACTIVE INGREDIENT SECTION

Glycerin, Hydrogen Peroxide, Purified Water

​Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12022-03712022-037-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
ec09f4e4-8539-793c-e053-2a95a90abbea94abe90d-70c5-45aa-b95b-8007f258f12f2022-10-27WarningsExact identifier
spl set id: 94abe90d-70c5-45aa-b95b-8007f258f12f

Reported adverse events (FAERS/openFDA)#

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