CoreTex Sun X SPF 30 New

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: CoreTex Sun X SPF 30 New
Generic name: AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Manufacturer: CoreTex Products Inc
Product type: HUMAN OTC DRUG
SPL set ID: 08fb4748-d22d-35af-e063-6394a90a0827
SPL ID: 08fb1bbf-f361-29da-e063-6394a90aa397
Version: 1
Effective date: 2023-10-30
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 05:48:03

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 2 · 53 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		CoreTex Sun X SPF 30 New	openfda.brand_name
generic name		AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	openfda.generic_name
manufacturer name		CoreTex Products Inc	openfda.manufacturer_name
ndc	package	65753-110-34	openfda.package_ndc
ndc	package	65753-110-18	openfda.package_ndc
ndc	package	65753-110-26	openfda.package_ndc
ndc	package	65753-110-40	openfda.package_ndc
ndc	package	65753-110-25	openfda.package_ndc
ndc	package	65753-110-04	openfda.package_ndc
ndc	package	65753-110-33	openfda.package_ndc
ndc	package	65753-110-02	openfda.package_ndc
ndc	package	65753-110-10	openfda.package_ndc
ndc	package	65753-110-37	openfda.package_ndc
ndc	package	65753-110-09	openfda.package_ndc
ndc	package	65753-110-01	openfda.package_ndc
ndc	package	65753-110-22	openfda.package_ndc
ndc	package	65753-110-03	openfda.package_ndc
ndc	package	65753-110-08	openfda.package_ndc
ndc	package	65753-110-05	openfda.package_ndc
ndc	package	65753-110-32	openfda.package_ndc
ndc	package	65753-110-07	openfda.package_ndc
ndc	package	65753-110-23	openfda.package_ndc
ndc	package	65753-110-24	openfda.package_ndc
ndc	package	65753-110-35	openfda.package_ndc
ndc	product	65753-110	openfda.product_ndc
ndc11	package	65753011035	derived:openfda.package_ndc
ndc11	package	65753011024	derived:openfda.package_ndc
ndc11	package	65753011037	derived:openfda.package_ndc
ndc11	package	65753011040	derived:openfda.package_ndc
ndc11	package	65753011004	derived:openfda.package_ndc
ndc11	package	65753011025	derived:openfda.package_ndc
ndc11	package	65753011009	derived:openfda.package_ndc
ndc11	package	65753011010	derived:openfda.package_ndc
ndc11	package	65753011002	derived:openfda.package_ndc
ndc11	package	65753011007	derived:openfda.package_ndc
ndc11	package	65753011023	derived:openfda.package_ndc
ndc11	package	65753011026	derived:openfda.package_ndc
ndc11	package	65753011034	derived:openfda.package_ndc
ndc11	package	65753011003	derived:openfda.package_ndc

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 on damaged or broken skin When using this product keep out of the eyes. Rinse with water to remove Stop use and ask a doctor if rash occurs Keep out of the 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.