TheraTears Lubricant

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 Lubricant
Generic name: CARBOXYMETHYLCELLULOSE SODIUM
Manufacturer: MEDTECH PRODUCTS INC
Product type: HUMAN OTC DRUG
SPL set ID: 797b0394-2f0f-4733-8d20-ec5bdf3e085d
SPL ID: 39e5aaf6-e4a0-4167-b458-f22af5906ddc
Version: 11
Effective date: 2025-10-23
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 02:12:33

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		TheraTears Lubricant	openfda.brand_name
generic name		CARBOXYMETHYLCELLULOSE SODIUM	openfda.generic_name
manufacturer name		MEDTECH PRODUCTS INC	openfda.manufacturer_name
ndc	package	58790-000-20	openfda.package_ndc
ndc	package	58790-000-24	openfda.package_ndc
ndc	package	58790-000-32	openfda.package_ndc
ndc	package	58790-000-00	openfda.package_ndc
ndc	package	58790-000-30	openfda.package_ndc
ndc	product	58790-000	openfda.product_ndc
ndc11	package	58790000032	derived:openfda.package_ndc
ndc11	package	58790000024	derived:openfda.package_ndc
ndc11	package	58790000000	derived:openfda.package_ndc
ndc11	package	58790000020	derived:openfda.package_ndc
ndc11	package	58790000030	derived:openfda.package_ndc
rxcui		2106821	openfda.rxcui
rxcui		1547948	openfda.rxcui
spl id		39e5aaf6-e4a0-4167-b458-f22af5906ddc	id
spl set id		797b0394-2f0f-4733-8d20-ec5bdf3e085d	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.