burton the nightmare before Christmas blurberry scented hand sanitizer
- Manufacturer
- BBC GROUP LIMITED | Townley Inc.
- Effective date
- 2018-07-20
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:52:27
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient purpose
Benzalkonium chloride 0.1% Antibacterial
Use
To decrease bacteria on the skin that could cause disease.
Warnings
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
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 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?
1-212-779-0544 weekdays
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Burton nightmare before christmas Raspberry scented hand sanitizer 01
- Benzalkonium Chloride
- COCETH-7
- PPG-1-PEG-9 LAURYL GLYCOL ETHER
- WATER O-18
- GLYCERIN
- CARBOMER 934
- SODIUM HYDROXIDE
- HYDROGENATED CASTOR OIL
- FD&C YELLOW NO. 5
- FD&C BLUE NO. 1
- MYRISTICA FRAGRANS FRUIT
- FD&C RED NO. 40
- D&C RED NO. 33
- BENZALKONIUM
- Burton nightmare before Christmas Grape scented hand sanitizer 01
- Burton nightmare before Christmas blueberry scented hand sanitizer 01
- POLYOXYL 40 HYDROGENATED CASTOR OIL
- Burton the nightmare before christmas blackberry scented hand sanitizer 01
- burton the nightmare before Christmas blurberry scented hand sanitizer 01
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 76383-001 | 76383-001-01 |
| 76383-002 | 76383-002-01 |
| 76383-003 | 76383-003-01 |
| 76383-004 | 76383-004-01 |
| 76383-005 | 76383-005-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 716b4431-c81d-537b-e053-2a95a90a033f | 716b4431-c81c-537b-e053-2a95a90a033f | 2018-07-20 | Warnings | 716b4431-c81d-537b-e053-2a95a90a033f 716b4431-c81c-537b-e053-2a95a90a033f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.




