HEB Lubricant Eye Drops

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: HEB Lubricant Eye Drops
Generic name: CARBOXYMETHYLCELLULOSE SODIUM
Manufacturer: HEB
Product type: HUMAN OTC DRUG
SPL set ID: 5d522e4d-d647-486f-a947-25c14b1417fa
SPL ID: 0cfaa286-19a1-c576-e063-6394a90a4af8
Version: 3
Effective date: 2023-12-20
Source export date: 2026-10-12
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:07:15

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		HEB Lubricant Eye Drops	openfda.brand_name
generic name		CARBOXYMETHYLCELLULOSE SODIUM	openfda.generic_name
manufacturer name		HEB	openfda.manufacturer_name
ndc	package	37808-100-01	openfda.package_ndc
ndc	product	37808-100	openfda.product_ndc
ndc11	package	37808010001	derived:openfda.package_ndc
rxcui		1188426	openfda.rxcui
spl id		0cfaa286-19a1-c576-e063-6394a90a4af8	id
spl set id		5d522e4d-d647-486f-a947-25c14b1417fa	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. Do not use this product if solution changes color or becomes cloudy When using the product do not reuse once opened, discard to avoid contamination, do not touch tip of container to any surface do not touch unit-dose tip to eye Stop use and ask a doctor if you experience eye pain changes in vision occur redness or irritation of the eye continues redness or irritation of the eye worsens or persists for more than 72 hours Keep out of reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Reported adverse events (FAERS/openFDA)#

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