REFRESH LACRI-LUBE

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: REFRESH LACRI-LUBE
Generic name: MINERAL OIL, PETROLATUM
Manufacturer: Allergan, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: d232a44b-516d-4cdf-a4e7-c3a9a50dc7af
SPL ID: b6d64a52-8a8a-4c90-ac67-41a32cc3c78a
Version: 8
Effective date: 2026-05-15
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:36:20

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		REFRESH LACRI-LUBE	openfda.brand_name
generic name		MINERAL OIL, PETROLATUM	openfda.generic_name
manufacturer name		Allergan, Inc.	openfda.manufacturer_name
ndc	package	0023-0312-07	openfda.package_ndc
ndc	package	0023-0312-04	openfda.package_ndc
ndc	product	0023-0312	openfda.product_ndc
ndc11	package	00023031207	derived:openfda.package_ndc
ndc11	package	00023031204	derived:openfda.package_ndc
rxcui		701984	openfda.rxcui
spl id		b6d64a52-8a8a-4c90-ac67-41a32cc3c78a	id
spl set id		d232a44b-516d-4cdf-a4e7-c3a9a50dc7af	set_id
unii		4T6H12BN9U	openfda.unii
unii		T5L8T28FGP	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 container to any surface. 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, or if the 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 right away.

Reported adverse events (FAERS/openFDA)#

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