FDA.reportPublic FDA data

RED GINSENG FERMENTED SUN

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2012-08-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:46:14

Label at a glance#

ProductRED GINSENG FERMENTED SUN SPF50PLUS PA PLUS PLUS PLUS
Active ingredientOCTINOXATE, ZINC OXIDE, TITANIUM DIOXIDE
Label structure8 sections

Indications and uses

How to Use: Shake the container before use. Apply an appropriate amount evenly to the areas of your skin that will be exposed to UV rays.

Dosage and administration

How to Use: Shake the container before use. Apply an appropriate amount evenly to the areas of your skin that will be exposed to UV rays.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Ethylhexyl Methoxycinnamate 7.3%, Zinc Oxide 4.3%, Titanium Dioxide 3.2%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Water, Cyclopentasiloxane, Cyclohexasiloxane, Saccharomyces/Panax Ginseng Root Ferment Filtrate, Dipropylene Glycol, Pentylene Glycol, Alcohol Denat., Dimethicone/Methicone Copolymer, Butylene Glycol, Aluminum Hydroxide, Stearic Acid, PEG-10 Dimethicone, Octocrylene, Cyclopentasiloxane, Dimethicone/Vinyl Dimethicone Crosspolymer, Ethylhexyl Palmitate, Silica, Neopentyl Glycol Diheptanoate, Niacinamide, Methyl Methacrylate Crosspolymer, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Caprylyl Methicone, Methyl Methacrylate Crosspolymer, Glyceryl Caprylate, Fragrance, Disteardimonium Hectorite, Caprylyl Glycol, Adenosine, Disodium EDTA, Dimethicone, Iron Oxides, Talc, Butylene Glycol, Glycyrrhiza Glabra (Licorice) Root Extract, Poria Cocos Extract, Ganoderma Lucidum (Mushroom) Extract, Panax Ginseng Root Extract, Astragalus Membranaceus Root Extract, Phenoxyethanol, Saccharomyces/Xylinum/Black Tea Ferment, Glycerin, Hydroxyethylcellulose, Phenoxyethanol, Potassium Sorbate, Carnosine

PURPOSE

OTC - PURPOSE SECTION

Purpose: This soft herbal sun liquid is designed to be not easily washed off from sweating and it does not leave a sticky residue on the skin.

WARNINGS

WARNINGS SECTION

Cautions:
For external use only.
Avoid contact with eyes and mouth.
Discontinue use if signs of irritation or rash appear.
Keep out of reach of children.
Replace the cap after use.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

How to Use: Shake the container before use. Apply an appropriate amount evenly to the areas of your skin that will be exposed to UV rays.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use: Shake the container before use. Apply an appropriate amount evenly to the areas of your skin that will be exposed to UV rays.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-020-012021-07-09C16284748780-19d75b9d0-5008-f424-e053-dadaa90a57ce1cef09b2-3d1c-4834-9100-89f46f1f9d27
51346-020-012020-01-31C16284748780-19d75b9d0-5008-f424-e053-dadaa90a57ce1cef09b2-3d1c-4834-9100-89f46f1f9d27

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z1
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RA1
CYCLOMETHICONE 5INACTIVE INGREDIENT0THT5PCI0R1
CYCLOMETHICONE 6INACTIVE INGREDIENTXHK3U310BA1
DIPROPYLENE GLYCOLINACTIVE INGREDIENTE107L85C401
PENTYLENE GLYCOLINACTIVE INGREDIENT50C1307PZG1

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-02051346-020-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIM
ZINC OXIDESOI2LOH54ZACTIM
TITANIUM DIOXIDE15FIX9V2JPACTIM
CYCLOMETHICONE 50THT5PCI0RIACT
CYCLOMETHICONE 6XHK3U310BAIACT
DIPROPYLENE GLYCOLE107L85C40IACT
PENTYLENE GLYCOL50C1307PZGIACT
BUTYLENE GLYCOL3XUS85K0RAIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 8 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
CYCLOMETHICONE 5CYCLOMETHICONE 50THT5PCI0RCREAM, AUGMENTED / TOPICAL260 mgExact identifier — unii candidate
3 equally ranked IID candidates
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates
CYCLOMETHICONE 5CYCLOMETHICONE 50THT5PCI0RAEROSOL / TOPICAL2.5 %w/wExact identifier — unii candidate
3 equally ranked IID candidates
CYCLOMETHICONE 5CYCLOMETHICONE 50THT5PCI0RAEROSOL, FOAM / TOPICAL144 mgExact identifier — unii candidate
3 equally ranked IID candidates
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / TRANSDERMAL296 mgExact identifier — unii candidate
3 equally ranked IID candidates
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40SYSTEM / TRANSDERMAL6 mgExact identifier — unii candidate
3 equally ranked IID candidates
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / BUCCAL30 mgExact identifier — unii candidate
3 equally ranked IID candidates

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
7713184e-b510-4efd-bdfc-2b3d3da2f7701cef09b2-3d1c-4834-9100-89f46f1f9d272021-07-08WarningsExact identifier
spl set id: 1cef09b2-3d1c-4834-9100-89f46f1f9d27

Reported adverse events (FAERS/openFDA)#

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