blink boost

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: blink boost
Generic name: GLYCERIN
Manufacturer: Bausch & Lomb Incorporated
Product type: HUMAN OTC DRUG
SPL set ID: e765c224-1718-488f-99b2-976eb60c1d63
SPL ID: 4f5f99fa-40c2-44a4-e063-6394a90a02be
Version: 4
Effective date: 2026-04-13
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:44

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		blink boost	openfda.brand_name
generic name		GLYCERIN	openfda.generic_name
manufacturer name		Bausch & Lomb Incorporated	openfda.manufacturer_name
ndc	package	29943-007-05	openfda.package_ndc
ndc	product	29943-007	openfda.product_ndc
ndc11	package	29943000705	derived:openfda.package_ndc
rxcui		2705824	openfda.rxcui
rxcui		2540675	openfda.rxcui
spl id		4f5f99fa-40c2-44a4-e063-6394a90a02be	id
spl set id		e765c224-1718-488f-99b2-976eb60c1d63	set_id
unii		PDC6A3C0OX	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 or becomes cloudy ■ if tamper evident ring is broken or missing When using this product ■ do not touch tip of container to any surface to avoid contamination ■ replace cap after using Stop use and ask a doctor if ■ you experience eye pain, changes in vision, continued redness or irritation of the eye ■ condition worsens or persists for more than 72 hours

Reported adverse events (FAERS/openFDA)#

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