FDA.reportPublic FDA data

NUVALU HAND SANITIZER GUAVA BURST 1OZ

Manufacturer
NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
Effective date
2021-03-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:48:30

Label at a glance#

ProductNUVALU HAND SANITIZER GUAVA BURST 1OZ
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Wet hands thoroughly with product and rub until dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

Label contents#

Full prescribing information#

Drug Facts Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70 percent

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Features

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin that could cause disease.
  • Recommended for repeated use.
  • Use anywhere without water.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and rub until dry without wiping.
  • For children under 6, use only under adult supervision.
  • Not recommended for infants.

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • Do not inhale or ingest.
  • Avoid contact with broken skin.

Other information

OTHER SAFETY INFORMATION

  • Do not store above 105 Fahrenheit
  • May discolor some fabrics
  • Harmful to wood finishes and plastics

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable. Keep away from heat and flame.
  • Discontinue if skin becomes irritated and ask a doctor.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Fragrance, Glycerin, Propylene Glycol, Triethanolamine, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, FD&C Red No.40, FD&C Yellow No.5

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-22776176-227-48

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
FD&C RED NO. 40WZB9127XOAIACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
CARBOMER 934Z135WT9208IACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
FD&C YELLOW NO. 5I753WB2F1MIACT

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
be5817eb-b5f3-47b2-e053-2a95a90a2be0be5815f9-15e8-6bee-e053-2a95a90a1c082021-03-01WarningsExact identifier
spl id: be5817eb-b5f3-47b2-e053-2a95a90a2be0
spl set id: be5815f9-15e8-6bee-e053-2a95a90a1c08

Reported adverse events (FAERS/openFDA)#

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