Dr. Butler Soothing Incontinence

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: Dr. Butler Soothing Incontinence
Generic name: PETROLATUM 36%
Manufacturer: Beyond Health P.A.
Product type: HUMAN OTC DRUG
SPL set ID: d17a0c28-a5b7-4df0-e053-2995a90a8edd
SPL ID: 2958cebe-650d-ea65-e063-6394a90a3f39
Version: 3
Effective date: 2024-12-15
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:49:21

Harmonized routes table
Harmonized routes
TOPICAL

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		Dr. Butler Soothing Incontinence	openfda.brand_name
generic name		PETROLATUM 36%	openfda.generic_name
manufacturer name		Beyond Health P.A.	openfda.manufacturer_name
ndc	package	70942-017-03	openfda.package_ndc
ndc	product	70942-017	openfda.product_ndc
ndc11	package	70942001703	derived:openfda.package_ndc
spl id		2958cebe-650d-ea65-e063-6394a90a3f39	id
spl set id		d17a0c28-a5b7-4df0-e053-2995a90a8edd	set_id
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

For external use only. Do not use on deep or puncture wounds. When using this product avoid contact in eyes, rinse with water to remove, contents under pressure, do not puncture or incinerate, do not store at temperatures above 120F. Stop use and ask a doctor if condition worsens, symptoms last more than 7 days or clear up and occur again within a few days. Ask a healthcare or professional before use.

Reported adverse events (FAERS/openFDA)#

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