U-MAX MULTI BB- allantoin cream

U-max Multi BB by

Drug Labeling and Warnings

U-max Multi BB by is a Otc medication manufactured, distributed, or labeled by VS Shinbi Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

active ingredient: allantoin

INACTIVE INGREDIENT

inactive ingredient:  macadamia ternifolia seed oil, simmondsia chinensis seed oil, cetyl ethylhexanoate, sorbitan sesquioleate, cetyl PEG/PPG10/1 dimethicone, ethylhexyl methoxycinnamate, hydrolyzed ellastin, butyl methoxydibenzoylmethane, shea butter, stearyl dimethicone, dimethicone, titanium dioxide, ci 77492, ci 77491, ci 44299, water, glycerin, butylene glycol, sodium chloride, hydrolyzed collagen, opuntia tuna fruit extract perform malt extract, houttuynia cordata extract, xanthium strumarium fruit extract, solanum lycopersicum fruit extract, clipta prostrata leaf extract, angelica gigas root extract, glycyrrhiza glabra root extract, camellia sinensis leaf extract, hydrolyzed soybean extract, artemisia vulgaris extract, laminaria japonica extract, taraxacum officinale leaf extract, citrus paradisi seed oil, musa sapientum fruit extract

PURPOSE

skin protectant (BB)

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

- apply only for skin
- apply 2 or 3 times a day with 5~6ml
- massage with your finger over 2 min and let them dry

WARNINGS

- keep out of eyes, ears and mouth
- if contact occurs, rinse away with plenty of cold water

DOSAGE & ADMINISTRATION

- for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

U-MAX MULTI BB 
allantoin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50795-2001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.1 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
MACADAMIA NUT (UNII: Y5432RGW8N)
HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
XANTHIUM STRUMARIUM FRUIT (UNII: TN770YC17C)
SOLANUM LYCOPERSICUM (UNII: 0243Q4990L)
ANGELICA GIGAS ROOT (UNII: 32766B2FHX)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
BANANA (UNII: 4AJZ4765R9)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
JOJOBA OIL (UNII: 724GKU717M)
LAMINARIA JAPONICA (UNII: WE98HW412B)
TARAXACUM OFFICINALE (UNII: 39981FM375)
CITRUS PARADISI SEED (UNII: 12F08874Y7)
CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
OCTINOXATE (UNII: 4Y5P7MUD51)
SHEA BUTTER (UNII: K49155WL9Y)
DIMETHICONE (UNII: 92RU3N3Y1O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50795-2001-1	30 mL in 1 BOTTLE, WITH APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/04/2012

Labeler - VS Shinbi Co., Ltd. (557817055)

Registrant - VS Shinbi Co., Ltd. (557817055)

Establishment
Name	Address	ID/FEI	Business Operations
VS Shinbi Co., Ltd.		557817055	manufacture