BUDDATE LOTUS MOISTURE ESSENCE

Manufacturer
BUDDATE Co Ltd
Effective date
2025-11-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:18:37

Label at a glance#

ProductBUDDATE LOTUS MOISTURE ESSENCE
Active ingredientPURSLANE, NIACINAMIDE, GLYCERIN, NELUMBO NUCIFERA FLOWER
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Glycerin: 5.93 %vv

Niacinamide: 2.00 %vv

Nelumbo Nucifera Flower Extract: 1.35 %vv

Portulaca Oleracea Extract: 0.50 %vv

INACTIVE INGREDIENT SECTION

Water, Butylene Glycol, Glycerin, Dipropylene Glycol, 1,2-Hexanediol, Niacinamide, Nelumbo Nucifera Flower Extract, Xylitylglucoside, Anhydroxylitol, Xylitol, Portulaca Oleracea Extract, Saccharide Isomerate, Biosaccharide Gum-1, Panthenol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tromethamine, Luffa Cylindrica Fruit Extract, Coix Lacryma-Jobi Ma-yuen Seed Extract, Ethylhexylglycerin, Hydrogenated Lecithin, Vigna Radiata Seed Extract, Cellulose Gum, Disodium EDTA, Sodium Hyaluronate, Ceramide 3, Glyceryl Acrylate/Acrylic Acid Copolymer, Camellia Sinensis Leaf Extract, Morus Bombycis Root Extract, Malva Sylvestris (Mallow) Extract, Mentha Piperita (Peppermint) Leaf Extract, Primula Veris Extract, Alchemilla Vulgaris Extract, Veronica Officinalis Extract, Melissa Officinalis Leaf Extract, Achillea Millefolium Extract

OTC - PURPOSE SECTION

Moisturrizer & Skin Conditioning (Protectant)

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

After applying a toner in the morning and in the evening, relieve a proper amount, spread it on the face smoothly and evenly from inside to the outside of the face and then gently pat for absorption.

WARNINGS SECTION

1. For external use only.

1) Do not use over the wound and irritated skin with eczema or infections

2) Discontinue using the product if signs of irritations and/or rashes occur and seek professional medical help

2. Keep the cover closed tight after use

3. Do not put the left over contents back into the container to avoid deterioration

1) Avoid contact with eyes

2) Keep out of reach of children

3) Store in a cool and dry place, away from direct sun light

DOSAGE & ADMINISTRATION SECTION

for external use only


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GLYCERIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71173-2000-12025-11-30C16284748780-12cef2736-5f4a-d83d-e063-dadaa90ab31fDrug Facts
71173-2000-12025-01-30C16284748780-12cef2736-5f4a-d83d-e063-dadaa90ab31fDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71173-2000-1BUDDATE LOTUS MOISTURE ESSENCE50 mL in 1 BOTTLE, PUMPLIQUID505

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71173-200071173-2000-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
BUDDATE LOTUS MOISTURE ESSENCEGLYCERIN, NIACINAMIDE, NELUMBO NUCIFERA FLOWER EXTRACT, PORTULACA OLERACEA EXTRACTBUDDATE Co Ltd46499995-8b13-3e5c-e054-00144ff88e882025-11-30WarningsExact identifier
ndc (package): 71173-2000-1
ndc (product): 71173-2000
ndc11 (package): 71173200001
spl id: 44cede31-8150-053d-e063-6394a90a0bc2
spl set id: 46499995-8b13-3e5c-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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