Watermelon hand sanitizer

Manufacturer
Zhejiang Meizhiyuan Cosmetics Co.,Ltd
Effective date
2022-11-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:46:41

Label at a glance#

ProductWatermelon hand sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Pump as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.

Storage and handling

Store at 20 o C (68 to 77 o F). May discolor fabrics.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v.

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin.

When water, soap & towel are not available.

Warnings

WARNINGS SECTION

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

Do not apply around eyes. Do not use in ear & mouth.

When using this product avoid contact with eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops and persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump as needed into your palms and thoroughly spread on both hands.
  • Rub into skin until dry.

Other information

STORAGE AND HANDLING SECTION

  • Store at 20 o C (68 to 77 oF).
  • May discolor fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (aqua), Aminomethyl propanol, Carbomer, Aloe Barbadensis (Aloe Vera) Gel, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), FD&C Yellow No. 5, FD&C Blue No. 1

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80204-027-012022-03-07C16284748780-1d6a99b39-fbc2-a426-e053-dadaa90af4c238ae8115-0f51-4f84-9b49-7cf658fa4c3a
80204-027-012022-01-28C16284748780-1d6a99b39-fbc2-a426-e053-dadaa90af4c238ae8115-0f51-4f84-9b49-7cf658fa4c3a

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80204-02780204-027-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
affc92ca-8b44-474f-be87-657804ab54dd38ae8115-0f51-4f84-9b49-7cf658fa4c3a2022-11-18WarningsExact identifier
spl id: affc92ca-8b44-474f-be87-657804ab54dd
spl set id: 38ae8115-0f51-4f84-9b49-7cf658fa4c3a

Reported adverse events (FAERS/openFDA)#

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