FDA.reportPublic FDA data

North Woods Derma Foam Hand Sanitizer

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
North Woods Derma Foam Hand Sanitizer
Generic name
BENZALKONIUM CHLORIDE
Manufacturer
Superior Chemical Corporation
Product type
HUMAN OTC DRUG
SPL set ID
ad51a175-2b91-fd14-e053-2995a90ad54d
SPL ID
408253ef-89cc-121e-e063-6294a90a24d4
Version
3
Effective date
2025-10-06
Source export date
2026-08-17
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-17/1428ecb25c316753060ea7ddb566e8693893fa6e325c185f8717828825c2afb3/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
ca19d5b1416b6b66a9d383bfdc77d90e91adfeefe16ffcc1ac6b06ceb90d8d73
Import run
20260818T065550Z
Imported at
2026-08-18 08:42:11
Harmonized routes table
Harmonized routes
TOPICAL

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. Avoid contact with eyes. Children under the age of 6 should be supervised by an adult when using this product. Discontinue use is irritation or redness develops. If irritation persists for more than 72 hours, consult a physician. KEEP OUT OF REACH OF CHILDREN .