BOTANIC HEAL BOH PROBIODERM REPAIR AMPOULE CUSHION 02 NATURAL BEIGE

Manufacturer
CJ OliveNetworks Co., Ltd. | Hankook Cosmetics Manufacturing Co.,Ltd_Eumseong Factory
Effective date
2019-08-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:15:52

Label at a glance#

ProductBOTANIC HEAL BOH PROBIODERM REPAIR AMPOULE CUSHION 02 NATURAL BEIGE
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, ZINC OXIDE, OCTOCRYLENE
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: TITANIUM DIOXIDE 9.00%, ETHYLHEXYL METHOXYCINNAMATE 7.00%, ETHYLHEXYL SALICYLATE 4.80%, ZINC OXIDE 2.00%, OCTOCRYLENE 2.00%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:
Water, Cyclopentasiloxane, Diphenylsiloxy Phenyl Trimethicone, Butylene Glycol, Propylene Glycol Dibenzoate, Lauryl PEG-10 Tris(Trimethylsiloxy)silylethyl Dimethicone, Caprylyl Methicone, Cetyl Ethylhexanoate, Cetyl PEG/PPG-10/1 Dimethicone, Pentaerythrityl Tetraisostearate, Niacinamide, Disteardimonium Hectorite, VP/Hexadecene Copolymer, Iron Oxides (CI 77492), Magnesium Sulfate, Mica(CI 77019), Caprylic/Capric Glycerides, Palmitic Acid, Stearic Acid, Iron Oxides (CI 77491), Triethoxycaprylylsilane, Aluminum Hydroxide, Parfum(Fragrance), Iron Oxides (CI 77499), Dimethicone/Vinyl Dimethicone Crosspolymer, Adenosine, Glycerin, Rosa Damascena Flower Water, Myristic Acid, 1,2-Hexanediol, Pearl Extract, Tocopherol, Caprylyl Glycol, Fucus Vesiculosus Extract, Prunella Vulgaris Extract, Lactobacillus Ferment, Phaseolus Angularis Seed Extract, Palmitoyl Tripeptide-5, Rosa Damascena Flower Oil, Acetyl Hexapeptide-8, Palmitoyl Tripeptide-1

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings:

For external use only. Avoid contact with eyes. Keep out of reach of children. Discontinue use if signs of irritation and/or rash appear.

DESCRIPTION

DESCRIPTION SECTION

Uses:
Helps protect skin from UV rays.

Directions:
Squeeze a moderate amount on a puff and apply to face along with the skin texture evenly as a foundation and gently stroke to get it absorbed.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71596-057-022021-07-01C16284748780-1ba0f9c33-3ca5-a910-e053-dadaa90a0b85b7f99699-810d-4418-8cd1-d7ad0362041d
71596-057-022021-01-29C16284748780-1ba0f9c33-3ca5-a910-e053-dadaa90a0b85b7f99699-810d-4418-8cd1-d7ad0362041d

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
71596-05771596-057-01, 71596-057-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
1a64e85a-b9aa-4017-9117-c081c9b594d8b7f99699-810d-4418-8cd1-d7ad0362041d2021-07-02WarningsExact identifier
spl set id: b7f99699-810d-4418-8cd1-d7ad0362041d

Reported adverse events (FAERS/openFDA)#

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