UV Capture Sun BB

Drug Labeling and Warnings

Drug Details [pdf]

UV CAPTURE SUN BB- titnium dioxide, ethylhexyl methoxycinnamate, zinc oxide cream 
Carver Korea Co.,Ltd

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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UV Capture Sun BB

• Active Ingredients: Purpose
• Titanium Dioxide 7.9%: Sunscreen
• Ethylhexyl Methoxycinnamate 3.0%: Sunscreen
• Zinc Oxide 1.9%: Sunscreen

Uses

- Helps prevent sunburn 

- If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warning

For external use only

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

- For sunscreen use:

- apply liberally 15 minutes before sun exposure 

- apply reapply at least every 2 hours Sun Protection Measures.

- children under 6 months: Ask a doctor

Dosage: Small Amount

Administration: apply to a clean skin and massage gently

WATER
PROPYLENE GLYCOL
DODECAMETHYLPENTASILOXANE
TALC
ISOPROPYL PALMITATE
HEXYLDECYL MYRISTOYL METHYLAMINOPROPIONATE
BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE
ALMOND OIL
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2)
DIPENTAERYTHRITYL HEXASTEARATE
ISOPROPYL ISOSTEARATE
NIACINAMIDE
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)
MAGNESIUM SULFATE
POLYGLYCERIN-4
TREHALOSE ISOSTEARATE ESTERS
BROWN IRON OXIDE
DISTEARDIMONIUM HECTORITE
PORTULACA OLERACEA WHOLE
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE)
PHENOXYETHANOL
TRIHYDROXYSTEARIN
METHICONE (20 CST)
TREHALOSE
HYDROXYETHYL STARCH 130/0.4
ETHYLHEXYLGLYCERIN
SILICA DIMETHYL SILYLATE
ALUMINUM HYDROXIDE
ALUMINUM STEARATE
ADENOSINE
ADANSONIA DIGITATA SEED OIL
.ALPHA.-BISABOLOL, (+)-
HYDROLYSED MARINE COLLAGEN (ENZYMATIC; 2000 MW)
OPUNTIA FICUS-INDICA
HYALURONATE SODIUM
VITIS VINIFERA SEED
DIOSPYROS KAKI LEAF
PINUS DENSIFLORA LEAF
CAMELLIA SINENSIS WHOLE
CENTELLA ASIATICA
CITRUS PARADISI FRUIT OIL
MELIA AZEDARACH WHOLE
ORYZA SATIVA WHOLE
PLATYCODON GRANDIFLORUM ROOT
POLYGALA TENUIFOLIA ROOT
SOPHORA FLAVESCENS ROOT
TARAXACUM OFFICINALE ROOT
BIOTINOYL TRIPEPTIDE-1
PALMITOYL OLIGOPEPTIDE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

UV CAPTURE SUN BB 
titnium dioxide, ethylhexyl methoxycinnamate, zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58930-062
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.37 g  in 30 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.90 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	0.57 g  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TALC (UNII: 7SEV7J4R1U)
NIACINAMIDE (UNII: 25X51I8RD4)
TREHALOSE (UNII: B8WCK70T7I)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ADENOSINE (UNII: K72T3FS567)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58930-062-01	30 mL in 1 TUBE; Type 0: Not a Combination Product	07/01/2014	12/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	07/01/2014	12/01/2018

Labeler - Carver Korea Co.,Ltd (688442290)

Registrant - Jemian USA Inc. (078822273)

Establishment
Name	Address	ID/FEI	Business Operations
Kolmar Korea Co., Ltd.		688732723	manufacture(58930-062)

Revised: 6/2019

Document Id: 28f8180d-8607-4eae-96dc-7f92e18247d7

34390-5

Set id: ff7d2985-5b5d-41af-a48e-ec8e4595de09

Version: 3

Effective Time: 20190611