BabyGanics Kids Alcohol Free Foaming Hand Sanitizer Berry Berry

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: BabyGanics Kids Alcohol Free Foaming Hand Sanitizer Berry Berry
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: KAS Direct LLC dba BabyGanics
Product type: HUMAN OTC DRUG
SPL set ID: 56b559c6-db10-47dd-9316-cc2d04cbef98
SPL ID: 7556506d-aa67-451b-a12c-93fae6d4a446
Version: 3
Effective date: 2025-12-08
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:54:42

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		BabyGanics Kids Alcohol Free Foaming Hand Sanitizer Cupcake	openfda.brand_name
brand name		BabyGanics Kids Alcohol Free Foaming Hand Sanitizer Berry Berry	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		KAS Direct LLC dba BabyGanics	openfda.manufacturer_name
ndc	package	59062-4200-1	openfda.package_ndc
ndc	package	59062-4100-1	openfda.package_ndc
ndc	product	59062-4100	openfda.product_ndc
ndc	product	59062-4200	openfda.product_ndc
ndc11	package	59062410001	derived:openfda.package_ndc
ndc11	package	59062420001	derived:openfda.package_ndc
spl id		7556506d-aa67-451b-a12c-93fae6d4a446	id
spl set id		56b559c6-db10-47dd-9316-cc2d04cbef98	set_id
unii		F5UM2KM3W7	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only When using this product avoid contact with eyes. In case of eye contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or redness develops, or if condition lasts for more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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