DEARDERM SPEED GEL VITAMIN C HAND SANITIZER- alcohol gel

DEARDERM SPEED gel Vitamin C Hand Sanitizer by

Drug Labeling and Warnings

DEARDERM SPEED gel Vitamin C Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Rainbow Co Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

alcohol

INACTIVE INGREDIENT

WATER
DIPROPYLENE GLYCOL
CARBOMER
GLYCERIN
TRIETHANOLAMINE
PEG-60 HYDROGENATED CASTOR OIL
PANTHENOL
CAMELLIA SINENSIS LEAF EXTRACT
ALOE 8AR8ADENSIS LEAF EXTRACT
DIETHANOLAMINE
CITRUS PARADIS! (GRAPEFRUIT) PEEL OIL

PURPOSE

Sterilization of hands and skin

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.

Supervise children in the use of this product.

WARNINGS

■ Flammable. Keep away from fire or flame.

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DEARDERM SPEED GEL VITAMIN C HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74247-0009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
GLYCERIN (UNII: PDC6A3C0OX)
GRAPEFRUIT PEEL (UNII: 3582N05Q44)
PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
DIETHANOLAMINE (UNII: AZE05TDV2V)
PANTHENOL (UNII: WV9CM0O67Z)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER 940 (UNII: 4Q93RCW27E)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74247-0009-1	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/01/2020

Labeler - Rainbow Co Ltd (690423720)

Registrant - Rainbow Co Ltd (690423720)

Establishment
Name	Address	ID/FEI	Business Operations
Rainbow Co Ltd		690423720	manufacture(74247-0009)