Mojito Sun description, usages, side effects, indications, overdosage, supplying and lots more!

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Mojito Sun

TRIZ LABORATORIES LTD

Drug Facts




FULL PRESCRIBING INFORMATION

Inactive Ingredients

Water, PEG-40 Hydrogenated Castor Oil, Acrylates/C10-30

Alkyl Acrylate Crosspolymer, DMDM Hydantoin, Parfum,

Sodium Hydroxide, Tocopherol Acetate,

Simmondsia, Chinensis

(Jojoba) Seed Wax,

FD and C Yellow 5 CI 19140, FD and C Blue 1 CI 42090

Active ingredient

Active Ingredient

Alcohol Denat 60 % w/w

Purpose

Purpose Antibacterial

Uses

Use - To decrease bacteria

on the skin and clean hands - Recommended

for repeated use

Warnings

For external use only.

Flammable, keep away from fire or flame

Keep Out of Reach of Children. If accidentally

swallowed, get medical help or contact a

Poison Control Center right away.

Do not get into eye. If contact

occurs, rinse thoroughly with water.

Discontinue use if irritation or redness

develops. If irritation persists for more than

72 hours, consult a doctor.

Directions - Apply to hands

until thoroughly wet. Rub

vigorously until dry.

Mojito Sun

Mojito Sun

ALCOHOL GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:53057-013
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALCOHOL ALCOHOL 18 mL

Inactive Ingredients

Ingredient Name Strength
water
POLYOXYL 40 HYDROGENATED CASTOR OIL
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
DMDM HYDANTOIN
SODIUM HYDROXIDE
.ALPHA.-TOCOPHEROL ACETATE
SIMMONDSIA CHINENSIS SEED WAX
FD&C YELLOW NO. 5
FD&C BLUE NO. 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:53057-013-01 30 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2014-05-13


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