RED PROPOLIS 30 VITA AMPULE

Manufacturer
Leejiham
Effective date
2020-09-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:16:31

Label at a glance#

ProductRED PROPOLIS 30 VITA AMPULE
Active ingredientGLYCERIN, NIACINAMIDE, PANTHENOL
Label structure11 sections

Indications and uses

for healthy-looking skin by caring antioxidant with red propolis extract and providing nourishment

Dosage and administration

After using a toner, apply 2~3 drops and gently pat to absorb

Storage and handling

Protect this product from direct sun and excessive heat

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Glycerin 5%

Panthenol 3%

Niacinamide 2%

Purpose

OTC - PURPOSE SECTION

Skin protectant

Whitening

Uses

DOSAGE & ADMINISTRATION SECTION

for healthy-looking skin by caring antioxidant with red propolis extract and providing nourishment

Warnings

WARNINGS SECTION

For external use only

Stop use and ask a physician

OTC - ASK DOCTOR SECTION

if skin irritation and redness occurs more than 72 hours.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help right away.

Directions

INDICATIONS & USAGE SECTION

After using a toner, apply 2~3 drops and gently pat to absorb

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propolis Extract, Methylpropanediol, Dipropylene Glycol, Glycerin, Panthenol, Niacinamide, Hydroxyacetophenone, Carbomer, Tromethamine, Caprylyl Glycol, Eclipta Prostrata Extract, Coccinia Indica Fruit Extract, 1,2-Hexanediol, Hyaluronic Acid Propanediol, Adenosine, Disodium EDTA, Benzyl Glycol, Hydrolyzed Glycosaminoglycans, Sodium Hyaluronate, Ethylhexylglycerin, Dipotassium Glycyrrhizate, Sodium Hyaluronate Crosspolymer, Magnesium Ascorbyl Phosphate, Ascorbic Acid, Hydrolyzed Hyaluronic Acid, Hydroxypropyltrimonium Hyaluronate, Sodium Acetylated Hyaluronate

Other information

STORAGE AND HANDLING SECTION

Protect this product from direct sun and excessive heat

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

35ml NDC: 80395-201-01 Label35ml NDC: 80395-201-01 Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80395-201-012022-06-14C16284748780-1d6a99b39-9467-a426-e053-dadaa90af4c280395-201
80395-201-012022-01-28C16284748780-1d6a99b39-9467-a426-e053-dadaa90af4c280395-201

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80395-20180395-201-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 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
e173fee9-fc99-b55c-e053-2995a90ae57eae3bd953-662a-32f4-e053-2a95a90a2fb92022-06-14WarningsExact identifier
spl set id: ae3bd953-662a-32f4-e053-2a95a90a2fb9

Reported adverse events (FAERS/openFDA)#

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