Droptics Dry Eye Relief

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: Droptics Dry Eye Relief
Generic name: CARBOXYMETHYLCELLULOSE SODIUM,GLYCERIN,POLYSORBATE 80
Manufacturer: Droptics LLC
Product type: HUMAN OTC DRUG
SPL set ID: 29d7614b-f4b7-48e2-97c5-d1bff27731d2
SPL ID: 57323f74-e0a0-1ad8-e063-6294a90ad9d4
Version: 5
Effective date: 2026-07-22
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:41

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		Droptics Dry Eye Relief	openfda.brand_name
generic name		CARBOXYMETHYLCELLULOSE SODIUM,GLYCERIN,POLYSORBATE 80	openfda.generic_name
manufacturer name		Droptics LLC	openfda.manufacturer_name
ndc	package	85211-002-02	openfda.package_ndc
ndc	package	85211-002-01	openfda.package_ndc
ndc	product	85211-002	openfda.product_ndc
ndc11	package	85211000201	derived:openfda.package_ndc
ndc11	package	85211000202	derived:openfda.package_ndc
rxcui		1241471	openfda.rxcui
spl id		57323f74-e0a0-1ad8-e063-6294a90ad9d4	id
spl set id		29d7614b-f4b7-48e2-97c5-d1bff27731d2	set_id
unii		PDC6A3C0OX	openfda.unii
unii		6OZP39ZG8H	openfda.unii
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 Do not use if solution changes color When using this product • Do not touch tip of the container to any surface to avoid contamination • Replace cap after each use Stop use and ask a doctor if • If you feel eye pain • Changes in vision occur • Redness or irritation of the eye lasts • Condition worsens or lasts more than 72 hours Keep out of reach of children • If 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.