MARVEL Spider-Man HAND SANITIZER With Case

Manufacturer
Huizhou Bliss Commodity Co., Ltd
Effective date
2020-10-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:04

Label at a glance#

ProductMARVEL Spider-Man HAND SANITIZER With Case
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 68%

Purpose

OTC - PURPOSE SECTION

 Antiseptic

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable.Keep away from heat or flame.
  • Discontinue if skin becomes irritated and ask a doctor
  • 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.
  • Do not inhale or ingest.
  • Avoid contact with broken skin.

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

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, propyene glycol, carbomer, sodium hydroxide, fragrance

SPL UNCLASSIFIED SECTION

Questions?

Call 1-800-684-1236

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1037039ethanol 68 % Topical GelPSN1
1037039ethanol 0.68 ML/ML Topical GelSCD1
1037039ethanol 68 % Topical GelSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74274-022-012024-07-30C16284748780-11030e365-6505-111a-e063-dadaa90a10e2020bd77b-0001-4994-8664-1b842786616b
74274-022-012024-01-30C16284748780-11030e365-6505-111a-e063-dadaa90a10e2020bd77b-0001-4994-8664-1b842786616b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74274-022-01MARVEL Spider-Man HAND SANITIZER With Case29 mL in 1 BOTTLEGEL291

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74274-022MARVEL SPIDER-MAN HAND SANITIZER WITH CASE (ALCOHOL) GEL [HUIZHOU BLISS COMMODITY CO., LTD]1Legacy NDC, 1 package rows20201007_020bd77b-0001-4994-8664-1b842786616b.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
74274-02274274-022-01

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
19b7f3f4-2e52-41a2-a44c-fa28c5045db8020bd77b-0001-4994-8664-1b842786616b2020-10-07WarningsExact identifier
spl id: 19b7f3f4-2e52-41a2-a44c-fa28c5045db8
spl set id: 020bd77b-0001-4994-8664-1b842786616b

Reported adverse events (FAERS/openFDA)#

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