Stream2Sea Broad Spectrum 20

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: Stream2Sea Broad Spectrum 20
Generic name: TITANIUM DIOXIDE
Manufacturer: Stream2Sea, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 1775d07d-6914-6928-e054-00144ff88e88
SPL ID: 42f52562-2470-9e85-e063-6294a90af104
Version: 10
Effective date: 2025-11-06
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:15:30

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 · 46 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		Stream2Sea Broad Spectrum 30 - Tinted	openfda.brand_name
brand name		Stream2Sea Broad Spectrum 30	openfda.brand_name
brand name		Stream2Sea Broad Spectrum 20 - Tinted	openfda.brand_name
brand name		Stream2Sea Broad Spectrum 20	openfda.brand_name
generic name		TITANIUM DIOXIDE	openfda.generic_name
manufacturer name		Stream2Sea, LLC	openfda.manufacturer_name
ndc	package	69555-021-60	openfda.package_ndc
ndc	package	69555-030-30	openfda.package_ndc
ndc	package	69555-030-32	openfda.package_ndc
ndc	package	69555-030-01	openfda.package_ndc
ndc	package	69555-031-91	openfda.package_ndc
ndc	package	69555-021-30	openfda.package_ndc
ndc	package	69555-021-90	openfda.package_ndc
ndc	package	69555-030-03	openfda.package_ndc
ndc	package	69555-020-32	openfda.package_ndc
ndc	package	69555-020-01	openfda.package_ndc
ndc	package	69555-031-30	openfda.package_ndc
ndc	package	69555-031-32	openfda.package_ndc
ndc	package	69555-030-33	openfda.package_ndc
ndc	package	69555-020-03	openfda.package_ndc
ndc	package	69555-021-32	openfda.package_ndc
ndc	package	69555-031-90	openfda.package_ndc
ndc	product	69555-030	openfda.product_ndc
ndc	product	69555-020	openfda.product_ndc
ndc	product	69555-021	openfda.product_ndc
ndc	product	69555-031	openfda.product_ndc
ndc11	package	69555002160	derived:openfda.package_ndc
ndc11	package	69555003190	derived:openfda.package_ndc
ndc11	package	69555003030	derived:openfda.package_ndc
ndc11	package	69555002001	derived:openfda.package_ndc
ndc11	package	69555003001	derived:openfda.package_ndc
ndc11	package	69555002032	derived:openfda.package_ndc
ndc11	package	69555002130	derived:openfda.package_ndc
ndc11	package	69555002190	derived:openfda.package_ndc
ndc11	package	69555003130	derived:openfda.package_ndc
ndc11	package	69555003003	derived:openfda.package_ndc
ndc11	package	69555002003	derived:openfda.package_ndc
ndc11	package	69555003132	derived:openfda.package_ndc
ndc11	package	69555003033	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. Stop use and ask a doctor if rash occurs. When using this product, keep out of eyes. RInse with water to remove.

Reported adverse events (FAERS/openFDA)#

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