Home DailyMed 3dd69bcb-3743-eb01-e063-6394a90ab7e0 Krx Aesthetics Biophase Molecular Night Peel Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer KRX RESOURCES SDN. BHD.
Effective date 2025-10-18
Label type HUMAN OTC DRUG LABEL
Version 3
Source full-release
Hydrated at 2026-06-01 01:39:31 Label at a glance# Product Krx Aesthetics Biophase Molecular Night Peel
Active ingredient SALICYLOYL PHYTOSPHINGOSINE, GLUCONOLACTONE
Label structure 8 sections
DailyMed Pharmacologic Classes# DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84755-0005-1 Krx Aesthetics Biophase Molecular Night Peel 2 U in 1 BOTTLE CREAM 2 3
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 20 matching rows.
Krx Aesthetics Biophase Molecular Night Peel BUTYLENE GLYCOL CAPRYLYL GLYCOL SODIUM HYALURONATE NIACINAMIDE ALLANTOIN BIOSACCHARIDE GUM-1 DIPROPYLENE GLYCOL WATER PANTHENOL HYDROXYACETOPHENONE ETHYLHEXYLGLYCERIN 1,2-HEXANEDIOL BETAINE PHENOXYETHANOL CHLORPHENESIN SALICYLOYL PHYTOSPHINGOSINE GLUCONOLACTONE PENTYLENE GLYCOL SODIUM CITRATE Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 19 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.