BUBBLE GUM HAND SANITIZER boy

Manufacturer
K7 Design Group Inc.
Effective date
2023-10-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:57:48

Label at a glance#

ProductBUBBLE GUM HAND SANITIZER boy
Active ingredientALCOHOL
Label structure6 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for hand-washing to decrease bacteria on the skin, only when water is not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flames

For external use only

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes.
  • if contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation and redness develop

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 allow to dry without wiping

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, fragrance, carbomer, triethanolamine, denatonium benzoate.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN3
581660ethanol 0.62 ML/ML Topical GelSCD3
581660ethanol 62 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74177-022-002022-10-10C16284748780-1d6a99b39-bfbc-a426-e053-dadaa90af4c2BUBBLE GUM HAND SANITIZER-boy
74177-022-002022-01-28C16284748780-1d6a99b39-bfbc-a426-e053-dadaa90af4c2BUBBLE GUM HAND SANITIZER-boy

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74177-022-00BUBBLE GUM HAND SANITIZER boy30 g in 1 BOTTLEGEL303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74177-022BUBBLE GUM HAND SANITIZER BOY (ALCOHOL) GEL [K7 DESIGN GROUP INC.]3Current NDC, Legacy NDC, 1 package rows20231026_a4e669d2-5482-7c20-e053-2995a90ab050.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74177-02274177-022-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML · Source PDF

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
BUBBLE GUM HAND SANITIZER boyALCOHOLK7 Design Group Inc.a4e669d2-5482-7c20-e053-2995a90ab0502023-10-26WarningsExact identifier
ndc (package): 74177-022-00
ndc (product): 74177-022
ndc11 (package): 74177002200
spl id: 0897c92f-ad36-a897-e063-6394a90af29c
spl set id: a4e669d2-5482-7c20-e053-2995a90ab050

Reported adverse events (FAERS/openFDA)#

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