NOON Cartessa Accelerate 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 Cartessa Accelerate Program
Generic name: ALLANTOIN, TITANIUM DIOXIDE, OCTOCRYLENE, AND AVOBENZONE
Manufacturer: Noon Aesthetics M.R. Ltd
Product type: HUMAN OTC DRUG
SPL set ID: 400ead81-ab07-400f-b261-db330e0fd004
SPL ID: 420bc181-b901-40b2-9022-67f113e5b60d
Version: 3
Effective date: 2025-01-14
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:04:34

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		NOON Cartessa Accelerate Program	openfda.brand_name
generic name		ALLANTOIN, TITANIUM DIOXIDE, OCTOCRYLENE, AND AVOBENZONE	openfda.generic_name
manufacturer name		Noon Aesthetics M.R. Ltd	openfda.manufacturer_name
ndc	package	78863-1270-2	openfda.package_ndc
ndc	package	78863-1230-2	openfda.package_ndc
ndc	package	78863-2700-1	openfda.package_ndc
ndc	product	78863-2700	openfda.product_ndc
ndc11	package	78863127002	derived:openfda.package_ndc
ndc11	package	78863123002	derived:openfda.package_ndc
ndc11	package	78863270001	derived:openfda.package_ndc
rxcui		241509	openfda.rxcui
spl id		420bc181-b901-40b2-9022-67f113e5b60d	id
spl set id		400ead81-ab07-400f-b261-db330e0fd004	set_id

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.

NOON Cartessa Accelerate Program

openFDA label record#

Harmonized identifier links#

Related Records#

Warnings cross-check#

warnings

warnings

Reported adverse events (FAERS/openFDA)#