Model AA-2012

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
Model AA-2012
Generic name
MODEL AA-2012
Manufacturer
AEROSPACE ACCESSORY SERVICE
Product type
HUMAN OTC DRUG
SPL set ID
e29b0f92-27b7-e09f-e053-2995a90a35e3
SPL ID
236e1247-19d0-e131-e063-6394a90a8c82
Version
3
Effective date
2024-10-01
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:44:42

Warnings cross-check#

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

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Antiseptic Wipes Warnings For external use only Do not use Do not use it in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor. Stop use and consult a doctor if the condition persists or gets worse. Do not use it for longer than 1 week unless directed by a doctor. Antiseptic Wipes Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

warnings

BZK Pads Warnings For external use only Do not use As an antiseptic for more than 1 week In the eyes Ask a Doctor before use if you have deep puncture wounds, animal bites, or serious burns Stop use and ask a doctor if irritation or redness develop Condition persistor gets worse Keep out of reach of children If swallowed get medical help or contact a Poison Control Center ( 1-800-222-1222) right away

Reported adverse events (FAERS/openFDA)#

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