Soothe Night Time

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 Night Time
Generic name: WHITE PETROLATUM MINERAL OIL
Manufacturer: Bausch & Lomb Incorporated
Product type: HUMAN OTC DRUG
SPL set ID: 638d3c3f-9960-43da-956e-0e28c77f533e
SPL ID: 22e15dc4-1977-7228-e063-6394a90a679a
Version: 8
Effective date: 2024-09-24
Source export date: 2026-09-28
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:14:17

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		Soothe Night Time	openfda.brand_name
generic name		WHITE PETROLATUM MINERAL OIL	openfda.generic_name
manufacturer name		Bausch & Lomb Incorporated	openfda.manufacturer_name
ndc	package	24208-313-34	openfda.package_ndc
ndc	product	24208-313	openfda.product_ndc
ndc11	package	24208031334	derived:openfda.package_ndc
rxcui		259196	openfda.rxcui
rxcui		1235262	openfda.rxcui
spl id		22e15dc4-1977-7228-e063-6394a90a679a	id
spl set id		638d3c3f-9960-43da-956e-0e28c77f533e	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 When using this product do not touch tip of container to any surface to avoid contamination do not use with contact lenses replace cap after use 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.