FDA.reportPublic FDA data

LANBELLE ULTRA LIFTING EGF AMPOULE

Manufacturer
Lanbelle, Inc. | Choice Cosmetic Co., Ltd
Effective date
2021-04-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:47:29

Label at a glance#

ProductLANBELLE ULTRA LIFTING EGF AMPOULE
Active ingredientALLANTOIN, GLYCERIN
Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Glycerin, Allantoin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30g30g

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81687-10181687-101-01, 81687-101-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
TERT-BUTYL ALCOHOLMD83SFE959IACT
BETAINE3SCV180C9WIACT
SODIUM ACETYLATED HYALURONATEWN66R7GL93IACT
ALLANTOIN344S277G0ZACTIB
ADENOSINEK72T3FS567IACT
GLYCERINPDC6A3C0OXACTIB
1,2-HEXANEDIOLTR046Y3K1GIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
WATER059QF0KO0RIACT
CAPRYLYL GLYCOL00YIU5438UIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATEKBC00G95HIIACT

Source Document#

Source XML

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
bfc3b089-3205-07ae-e053-2995a90a46e7bd14acea-cd27-9cfb-e053-2a95a90a95752021-04-12Exact identifier
spl id: bfc3b089-3205-07ae-e053-2995a90a46e7
spl set id: bd14acea-cd27-9cfb-e053-2a95a90a9575

Reported adverse events (FAERS/openFDA)#

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