Equate Nighttime Relief Lubricant

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: Equate Nighttime Relief Lubricant
Generic name: LIGHT MINERAL OIL, WHITE PETROLATUM
Manufacturer: Walmart
Product type: HUMAN OTC DRUG
SPL set ID: 4449a55b-2cd4-0cb9-e063-6294a90aafbc
SPL ID: 465c2f6a-4aeb-94fc-e063-6294a90a2150
Version: 2
Effective date: 2025-12-20
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:29:24

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		Equate Nighttime Relief Lubricant	openfda.brand_name
generic name		LIGHT MINERAL OIL, WHITE PETROLATUM	openfda.generic_name
manufacturer name		Walmart	openfda.manufacturer_name
ndc	package	79903-367-01	openfda.package_ndc
ndc	product	79903-367	openfda.product_ndc
ndc11	package	79903036701	derived:openfda.package_ndc
rxcui		702008	openfda.rxcui
spl id		465c2f6a-4aeb-94fc-e063-6294a90a2150	id
spl set id		4449a55b-2cd4-0cb9-e063-6294a90aafbc	set_id
unii		N6K5787QVP	openfda.unii
unii		B6E5W8RQJ4	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

WARNING For External Use Only Do not use ■ except under the advice and supervision of a doctor When using this product ■replace cap after use to avoid contamination ■do not touch tip of container to any surface remove contact lenses before 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.