DR. YOUNG 2P PEARL BRIGHTENING BALM SPF35 PA- allantoin cream

Dr. Young 2P Pearl Brightening Balm SPF35 PA by

Drug Labeling and Warnings

Dr. Young 2P Pearl Brightening Balm SPF35 PA by is a Otc medication manufactured, distributed, or labeled by The Doctors Cosmetics Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

allantoin

INACTIVE INGREDIENT

water, cyclopentasiloxane, cyclohexasiloxane, titanium dioxide, ethylhexyl methoxycinnamate, glycerin, dipropylene glycol, hexyl laurate, butylene glycol dicaprylate / dicaprate, cytyl peg/ppg-10/1 dimethicone, bentonite, chrysanthellum indicum extract, magnesium sulfate, zinc oxide, pearl powder, magnolia liliflora flower extract, lilium candidum flower extract, convallaria majalis bulb/root extract, shea butter, magnolia kobus bark extract, ghujopsis dolabrata branch extract, camellia sinensis leaf extract, grapefruit fruit extract, centella asiatica extract, althaea rosea flower extract, aloe barbadensis leaf extract, silica, triethoxycaprylsilane, ci 77492, ci 77491, ci 44299, ultramarines, sorbitan siostearate, tocopheryl acetate, ascorbyl glucoside, lilium candidum flower extract, ceramide 3, disodium edta, methylparaben, propylparaben, fragrance

PURPOSE

UVB, UVA protection

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

After basic skin care routine, apply evenly to your face

WARNINGS

When using this product
- keep out of eyes, ears, and mouth.  If contact occurs, rinse with plenty of cold water right away and contact a physician.  If swallowing, drink plenty of water and contact a physician

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR. YOUNG 2P PEARL BRIGHTENING BALM SPF35 PA 
allantoin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43948-1101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.5 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
OCTINOXATE (UNII: 4Y5P7MUD51)
GLYCERIN (UNII: PDC6A3C0OX)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
HEXYL LAURATE (UNII: 4CG9F9W01Q)
BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)
BENTONITE (UNII: A3N5ZCN45C)
CHRYSANTHELLUM INDICUM FLOWER OIL (UNII: HJ299SUZ05)
MAGNESIUM SULFATE (UNII: DE08037SAB)
ZINC OXIDE (UNII: SOI2LOH54Z)
MAGNOLIA LILIIFLORA FLOWER (UNII: SVM28292LH)
CONVALLARIA MAJALIS BULB (UNII: 261W7X975U)
SHEA BUTTER (UNII: K49155WL9Y)
MAGNOLIA KOBUS BARK (UNII: 54LVP49595)
THUJOPSIS DOLABRATA WHOLE (UNII: Q190548W6J)
BANCHA TEA LEAF/TWIG (UNII: EWI42IEH1C)
PUMMELO (UNII: ET1TN5W71X)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
ALCEA ROSEA FLOWER (UNII: 1250O8MKPZ)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
LILIUM CANDIDUM FLOWER (UNII: COV655U2CJ)
CERAMIDE 3 (UNII: 4370DF050B)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43948-1101-1	30 mL in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	09/27/2012

Labeler - The Doctors Cosmetics Co., Ltd (687479378)

Registrant - The Doctors Cosmetics Co., Ltd (687479378)

Establishment
Name	Address	ID/FEI	Business Operations
The Doctors Cosmetics Co., Ltd		687479378	manufacture(43948-1101)