Silicea

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: Silicea
Generic name: SILICON DIOXIDE
Manufacturer: Hyland's Inc.
Product type: HUMAN OTC DRUG
SPL set ID: d3c426ab-1a61-3494-e053-2a95a90a9677
SPL ID: efcdac0e-3ad9-d79a-e053-2995a90a128d
Version: 2
Effective date: 2022-12-14
Source export date: 2026-10-27
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/eeb012fd0992efa4f76b2aef09dd5f84150b96392c46717c44deabcc4e3581c1/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:45:57

Harmonized routes table
Harmonized routes
ORAL

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Silicea	openfda.brand_name
generic name		SILICON DIOXIDE	openfda.generic_name
manufacturer name		Hyland's Inc.	openfda.manufacturer_name
ndc	package	54973-4083-1	openfda.package_ndc
ndc	package	54973-4083-2	openfda.package_ndc
ndc	product	54973-4083	openfda.product_ndc
ndc11	package	54973408301	derived:openfda.package_ndc
ndc11	package	54973408302	derived:openfda.package_ndc
spl id		efcdac0e-3ad9-d79a-e053-2995a90a128d	id
spl set id		d3c426ab-1a61-3494-e053-2a95a90a9677	set_id
unii		ETJ7Z6XBU4	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 Stop use and ask a doctor if ■ symptoms persist for more than 7 days or worsen. ■ irritation, pain, swelling or redness persists or worsens. If pregnant or breastfeeding ask a health professional before use. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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