NOON Post Procedure Program

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
NOON Post Procedure Program
Generic name
ALLANTOIN, TITANIUM DIOXIDE, OCTOCRYLENE, AND AVOBENZONE
Manufacturer
Noon Aesthetics M.R. Ltd
Product type
HUMAN OTC DRUG
SPL set ID
9d1d11b4-40ff-4ea8-a3af-655f457c05f1
SPL ID
e4aba8d5-9ace-499f-9db8-25a63bc946e5
Version
3
Effective date
2025-01-14
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:46:20

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

Warnings For external use only. Do not use on deep or puncture wounds, animal bites, serious burns. When using this product avoid contact with eyes. In case of eye contact, flush with water. Stop use and ask a doctor if condition worsens. symptoms last more than 7 days or clear up and occur again within a few days. Keep out of reach of children.

warnings

Warnings For external use only. Do not use on damage or broken skin. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash or irritation develops and lasts. Keep out of reach of children. If product is 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.