Indications and uses
How to Use: Apply an appropriate amount to the face with a puff provided in the package.
PLACENTA EX ESSENCE BB
- Manufacturer
- NATURE REPUBLIC CO., LTD.
- Effective date
- 2012-08-26
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 01:46:15
Label at a glance#
ProductPLACENTA EX ESSENCE BB SPF50PLUS PA PLUS PLUS PLUS
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE
Label structure8 sections
Dosage and administration
How to Use: Apply an appropriate amount to the face with a puff provided in the package.
Label contents#
Full prescribing information#
ACTIVE INGREDIENT
Active Ingredients: Titanium Dioxide 13.81%, Ethylhexyl Methoxycinnamate 7%, Zinc Oxide 3.92%
INACTIVE INGREDIENT
Inactive Ingredients:
Water, Cyclopentasiloxane, Cyclohexasiloxane, Triethoxycaprylylsilane, Aluminum Hydroxide, Stearic Acid, Dimethicone, Butylene Glycol Dicaprylate/Dicaprate, Butylene Glycol, Phenyl Trimethicone, Glycerin, Arbutin, Cetyl PEG/PPG-10/1 Dimethicone, Pentylene Glycol, Sodium Chloride, Methyl Methacrylate Crosspolymer, Hexyl Laurate, Isoamyl p-Methoxycinnamate, Cyclopentasiloxane, Dimethicone/Vinyl Dimethicone Crosspolymer, Sorbitan Sesquioleate, Iron Oxides, Triethoxycaprylylsilane, Polyglyceryl-4 Isostearate, Disteardimonium Hectorite, Cetyl Dimethicone, Ozokerite, Glycine Soja (Soybean)Phytoplacenta Extract, Beeswax, Phenoxyethanol, Ethylhexylglycerin, Fragrance, Portulaca Oleracea Extract, 1,2-Hexanediol, Hydrolyzed Collagen, Disodium EDTA, Adenosine, Citrus Aurantium Dulcis (Orange) Fruit Water, Alcohol, Gentiana Lutea Root Extract, Achillea Millefolium Extract, Artemisia Absinthium Extract, Arnica Montana Flower Extract, Potassium Sorbate
PURPOSE
Purpose: Moistful BB cream with multi-functions of brightening, anti-aging care and UV protection.
WARNINGS
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
KEEP OUT OF REACH OF CHILDREN
INDICATIONS AND USAGE
How to Use: Apply an appropriate amount to the face with a puff provided in the package.
DOSAGE AND ADMINISTRATION
How to Use: Apply an appropriate amount to the face with a puff provided in the package.
PACKAGE LABEL. PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 51346-030-01 | 2021-07-09 | C162847 | 48780-1 | 9d75b9d0-fd2d-f424-e053-dadaa90a57ce | 7010e1cb-1d99-4ef2-9b88-3f2cb4899471 |
| 51346-030-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-fd2d-f424-e053-dadaa90a57ce | 7010e1cb-1d99-4ef2-9b88-3f2cb4899471 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| OCTINOXATE | ACTIVE INGREDIENT | 4Y5P7MUD51 | 1 | |
| TITANIUM DIOXIDE | ACTIVE INGREDIENT | 15FIX9V2JP | 1 | |
| ZINC OXIDE | ACTIVE INGREDIENT | SOI2LOH54Z | 1 | |
| OCTINOXATE | ACTIVE MOIETY | 4Y5P7MUD51 | 1 | |
| TITANIUM DIOXIDE | ACTIVE MOIETY | 15FIX9V2JP | 1 | |
| ZINC OXIDE | ACTIVE MOIETY | SOI2LOH54Z | 1 | |
| ALUMINUM HYDROXIDE | INACTIVE INGREDIENT | 5QB0T2IUN0 | 1 | |
| CYCLOMETHICONE 5 | INACTIVE INGREDIENT | 0THT5PCI0R | 1 | |
| CYCLOMETHICONE 6 | INACTIVE INGREDIENT | XHK3U310BA | 1 | |
| TRIETHOXYCAPRYLYLSILANE | INACTIVE INGREDIENT | LDC331P08E | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- PLACENTA EX ESSENCE BB SPF50PLUS PA PLUS PLUS PLUS
- TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE
- TITANIUM DIOXIDE
- OCTINOXATE
- ZINC OXIDE
- WATER
- CYCLOMETHICONE 5
- CYCLOMETHICONE 6
- TRIETHOXYCAPRYLYLSILANE
- ALUMINUM HYDROXIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 51346-030 | 51346-030-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| TITANIUM DIOXIDE | 15FIX9V2JP | ACTIM |
| OCTINOXATE | 4Y5P7MUD51 | ACTIM |
| ZINC OXIDE | SOI2LOH54Z | ACTIM |
| WATER | 059QF0KO0R | IACT |
| CYCLOMETHICONE 5 | 0THT5PCI0R | IACT |
| CYCLOMETHICONE 6 | XHK3U310BA | IACT |
| TRIETHOXYCAPRYLYLSILANE | LDC331P08E | IACT |
| ALUMINUM HYDROXIDE | 5QB0T2IUN0 | IACT |
Source Document#
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| ALUMINUM HYDROXIDE | ALUMINUM HYDROXIDE | 5QB0T2IUN0 | OINTMENT / TOPICAL | NA | ||
| CYCLOMETHICONE 5 | CYCLOMETHICONE 5 | 0THT5PCI0R | CREAM, AUGMENTED / TOPICAL | 260 mg | ||
| ALUMINUM HYDROXIDE | ALUMINUM HYDROXIDE | 5QB0T2IUN0 | CREAM / TOPICAL | 5 %w/w | ||
| ALUMINUM HYDROXIDE | ALUMINUM HYDROXIDE | 5QB0T2IUN0 | CAPSULE / ORAL | NA | ||
| CYCLOMETHICONE 5 | CYCLOMETHICONE 5 | 0THT5PCI0R | AEROSOL, FOAM / TOPICAL | 144 mg | ||
| ALUMINUM HYDROXIDE | ALUMINUM HYDROXIDE | 5QB0T2IUN0 | TABLET / ORAL | 50 mg | ||
| CYCLOMETHICONE 5 | CYCLOMETHICONE 5 | 0THT5PCI0R | AEROSOL / TOPICAL | 2.5 %w/w |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 61e9387e-b15d-47af-bf21-2cb0c614e666 | 7010e1cb-1d99-4ef2-9b88-3f2cb4899471 | 2021-07-08 | Warnings | 7010e1cb-1d99-4ef2-9b88-3f2cb4899471 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.