FDA.reportPublic FDA data

my little pony cotton candy scented hand sanitizer

Manufacturer
BBC GROUP LIMITED | Townley Inc.
Effective date
2018-08-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:52:27

Label at a glance#

Productmy little pony cotton candy scented hand sanitizer 01
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Label contents#

Full prescribing information#

Active ingredient purpose

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1% Antibacterial

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease.

Warnings

WARNINGS SECTION

For external use only-hands

keep out of eyes- avoid contact with broken skin

Stop use and ask a dosctor if irritation or radness develops

Do not inhale or ingest. If swallowed, get medical help or contact a poison control right away.

Direction

DOSAGE & ADMINISTRATION SECTION

Rub a dime sized drop into hands.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

For children under 6 use under adult supervision

Inactive ingredients

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: WATER, GLYCERIN, COCETH-7, PPG-1-PEG-9 LAURYL GLYCOL ETHER, CARBOMER, SODIUM HYDROXIDE, PEG-40 HYDROGENATED CASTOR OIL, FRAGRANCE (PARFUM).
MAY CONTAIN: RED 40, RED 33, BLUE 1, YELLOW 5.

Questions?

OTC - QUESTIONS SECTION

1-212-779-0544 weekdays

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

76383-006-0176383-006-0176383-007-0176383-007-01

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130719565379888GTIN-13: 0719565379888
EAN-13: 0719565379888
GTIN-12: 719565379888
UPC-A: 719565379888
GTIN storage (14 digits): 00719565379888		MP0039WA_0706-min.jpg
BarcodeEAN-130719565379895GTIN-13: 0719565379895
EAN-13: 0719565379895
GTIN-12: 719565379895
UPC-A: 719565379895
GTIN storage (14 digits): 00719565379895		MP0040WA_0706-min.jpg

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76383-00676383-006-01
76383-00776383-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
COCETH-758Y261JLH5IACT
PPG-1-PEG-9 LAURYL GLYCOL ETHER5R8J43K25LIACT
WATER O-187QV8F8BYNJIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER 934Z135WT9208IACT
SODIUM HYDROXIDE55X04QC32IIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
MYRISTICA FRAGRANS FRUITGOO22BTU71IACT
FD&C RED NO. 40WZB9127XOAIACT
D&C RED NO. 339DBA0SBB0LIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
GLYCERINPDC6A3C0OXIACT
COCETH-758Y261JLH5IACT
PPG-1-PEG-9 LAURYL GLYCOL ETHER5R8J43K25LIACT
CARBOMER 934Z135WT9208IACT
SODIUM HYDROXIDE55X04QC32IIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
WATER O-187QV8F8BYNJIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
MYRISTICA FRAGRANS FRUITGOO22BTU71IACT
D&C RED NO. 339DBA0SBB0LIACT
FD&C RED NO. 40WZB9127XOAIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
74907a0a-57dc-e801-e053-2a91aa0a50f074907a0a-57db-e801-e053-2a91aa0a50f02018-08-29WarningsExact identifier
spl id: 74907a0a-57dc-e801-e053-2a91aa0a50f0
spl set id: 74907a0a-57db-e801-e053-2a91aa0a50f0

Reported adverse events (FAERS/openFDA)#

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