Soothe XP Preservative Free

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: Soothe XP Preservative Free
Generic name: LIGHT MINERAL OIL AND MINERAL OIL
Manufacturer: Bausch & Lomb Incorporated
Product type: HUMAN OTC DRUG
SPL set ID: b254d885-6d49-4c95-b6be-cfdad49c85e6
SPL ID: 2298b766-e9e4-0319-e063-6394a90a50dc
Version: 6
Effective date: 2024-09-20
Source export date: 2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:53:29

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		Soothe XP Preservative Free	openfda.brand_name
generic name		LIGHT MINERAL OIL AND MINERAL OIL	openfda.generic_name
manufacturer name		Bausch & Lomb Incorporated	openfda.manufacturer_name
ndc	package	24208-742-99	openfda.package_ndc
ndc	package	24208-742-01	openfda.package_ndc
ndc	product	24208-742	openfda.product_ndc
ndc11	package	24208074299	derived:openfda.package_ndc
ndc11	package	24208074201	derived:openfda.package_ndc
rxcui		1594962	openfda.rxcui
rxcui		577927	openfda.rxcui
spl id		2298b766-e9e4-0319-e063-6394a90a50dc	id
spl set id		b254d885-6d49-4c95-b6be-cfdad49c85e6	set_id
unii		N6K5787QVP	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 Do not use if solution changes color if single-unit dispenser is not intact When using this product do not touch the tip of container to any surface to avoid contamination once opened, discard do not reuse Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if 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.