TheraTears

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: TheraTears
Generic name: CARBOXYMETHYLCELLULOSE SODIUM
Manufacturer: MEDTECH PRODUCTS INC
Product type: HUMAN OTC DRUG
SPL set ID: 17a01236-130f-495b-9f8d-92b6a23b2dc5
SPL ID: 5b0f0fc3-3f46-4acb-e063-6294a90a72af
Version: 12
Effective date: 2026-09-09
Source export date: 2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:07:58

Harmonized routes table
Harmonized routes
OPHTHALMIC

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		TheraTears	openfda.brand_name
generic name		CARBOXYMETHYLCELLULOSE SODIUM	openfda.generic_name
manufacturer name		MEDTECH PRODUCTS INC	openfda.manufacturer_name
ndc	package	58790-002-28	openfda.package_ndc
ndc	package	58790-003-30	openfda.package_ndc
ndc	product	58790-002	openfda.product_ndc
ndc	product	58790-003	openfda.product_ndc
ndc11	package	58790000330	derived:openfda.package_ndc
ndc11	package	58790000228	derived:openfda.package_ndc
rxcui		579907	openfda.rxcui
rxcui		998666	openfda.rxcui
spl id		5b0f0fc3-3f46-4acb-e063-6294a90a72af	id
spl set id		17a01236-130f-495b-9f8d-92b6a23b2dc5	set_id
unii		K679OBS311	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 To avoid contamination do not touch tip of opened container to any surface. Do not reuse. Once opened discard. Use individual vials within 90 days of opening foil pouch. This product contains no preservatives. Any solution not used immediately after opening should be discarded. Re-use of this single-use product may lead to inflammation of the eye and/or discomfort, based on potential contamination during handling. Do not use If solution changes color or becomes cloudy. Stop use and ask a doctor if You experience eye pain, changes in vision, continued redness or irritation. Condition worsens or persists for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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