Sombra Max

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: Sombra Max
Generic name: SOMBRA MAX
Manufacturer: Sombra Cosmetics Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 41623a46-e6e7-907e-e063-6394a90afc4c
SPL ID: 41623a46-e6e8-907e-e063-6394a90afc4c
Version: 1
Effective date: 2025-10-17
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:29

Harmonized routes table
Harmonized routes
TOPICAL

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Sombra Max	openfda.brand_name
generic name		SOMBRA MAX	openfda.generic_name
manufacturer name		Sombra Cosmetics Inc.	openfda.manufacturer_name
ndc	package	61577-3440-2	openfda.package_ndc
ndc	package	61577-3440-1	openfda.package_ndc
ndc	product	61577-3440	openfda.product_ndc
ndc11	package	61577344002	derived:openfda.package_ndc
ndc11	package	61577344001	derived:openfda.package_ndc
spl id		41623a46-e6e8-907e-e063-6394a90afc4c	id
spl set id		41623a46-e6e7-907e-e063-6394a90afc4c	set_id
unii		3POA0Q644U	openfda.unii
unii		S07O44R1ZM	openfda.unii
unii		5TJD82A1ET	openfda.unii
unii		WW64GZ6LQY	openfda.unii
unii		LAV5U5022Y	openfda.unii

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. Do not use if allergic to salicylates (including aspirin), on wounds or damaged skin or with a heat source. When using this product: avoid bandaging tightly, avoid contact with eyes, keep out of reach of children. If swallowed, get medical help or contact a Posion Control Center right away. Stop use and ask doctor if: condition worsens, symptoms persist for more than 7 days, clear up and occur again within a few days.

Reported adverse events (FAERS/openFDA)#

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