Soft and Silky Antiseptic

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: Soft and Silky Antiseptic
Generic name: ANTISEPTIC LOTION SOAP
Manufacturer: Kutol Products Company, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 09d96b8d-be13-4295-8110-98dd82a454fa
SPL ID: 298df384-7077-6a74-e063-6394a90aecb5
Version: 6
Effective date: 2024-12-18
Source export date: 2026-10-30
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/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:39:15

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 · 26 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Soft and Silky Antiseptic	openfda.brand_name
generic name		ANTISEPTIC LOTION SOAP	openfda.generic_name
manufacturer name		Kutol Products Company, Inc.	openfda.manufacturer_name
ndc	package	50865-025-65	openfda.package_ndc
ndc	package	50865-025-09	openfda.package_ndc
ndc	package	50865-025-93	openfda.package_ndc
ndc	package	50865-025-80	openfda.package_ndc
ndc	package	50865-025-82	openfda.package_ndc
ndc	package	50865-025-07	openfda.package_ndc
ndc	package	50865-025-12	openfda.package_ndc
ndc	package	50865-025-18	openfda.package_ndc
ndc	package	50865-025-03	openfda.package_ndc
ndc	product	50865-025	openfda.product_ndc
ndc11	package	50865002518	derived:openfda.package_ndc
ndc11	package	50865002509	derived:openfda.package_ndc
ndc11	package	50865002593	derived:openfda.package_ndc
ndc11	package	50865002503	derived:openfda.package_ndc
ndc11	package	50865002580	derived:openfda.package_ndc
ndc11	package	50865002582	derived:openfda.package_ndc
ndc11	package	50865002512	derived:openfda.package_ndc
ndc11	package	50865002507	derived:openfda.package_ndc
ndc11	package	50865002565	derived:openfda.package_ndc
spl id		298df384-7077-6a74-e063-6394a90aecb5	id
spl set id		09d96b8d-be13-4295-8110-98dd82a454fa	set_id
unii		0F32U78V2Q	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 in the eyes. In case of contact, immediately flush with water. Stop use and ask a doctor if irritation or rash appears and lasts. 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.