Peannuts Hand Sanitizer

Manufacturer
Huizhou Bliss Commodity Co., Ltd
Effective date
2020-12-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:34:29

Label at a glance#

ProductPeannuts Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

To decrease bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 68%

Purpose

OTC - PURPOSE SECTION

 Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin that could cause disease.
  • Recommended for repeated use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

warnings:

WARNINGS SECTION

  • Flamable, keep away from heat and flame
  • For external use only.
  • Discontinue if skin away from heat and flame.
  • Keep out of reach of children
  • In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately

When using this product

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

Other Information:

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Propylene Glycol, Sodium Hydroxide, Fragrance

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286291ethanol 68 % Topical SolutionPSN1
2286291ethanol 0.68 ML/ML Topical SolutionSCD1
2286291ethanol 68 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74274-120-012024-07-30C16284748780-11030e365-3aba-111a-e063-dadaa90a10e2599bef57-5c8a-4bb7-b277-3988083aaf85
74274-120-012024-01-30C16284748780-11030e365-3aba-111a-e063-dadaa90a10e2599bef57-5c8a-4bb7-b277-3988083aaf85

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74274-120-01Peannuts Hand Sanitizer29 mL in 1 BOTTLELIQUID291

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74274-120PEANNUTS HAND SANITIZER (ALCOHOL) LIQUID [HUIZHOU BLISS COMMODITY CO., LTD]1Legacy NDC, 1 package rows20201203_599bef57-5c8a-4bb7-b277-3988083aaf85.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74274-12074274-120-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
05f4fae0-bed8-4b27-ad4a-4fa146c8d922599bef57-5c8a-4bb7-b277-3988083aaf852020-12-03WarningsExact identifier
spl id: 05f4fae0-bed8-4b27-ad4a-4fa146c8d922
spl set id: 599bef57-5c8a-4bb7-b277-3988083aaf85

Reported adverse events (FAERS/openFDA)#

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