MARVEL SPIDERMAN HAND SANITIZER WITH CASE- alcohol solution

Marvel Spiderman Hand Sanitizer With Case by

Drug Labeling and Warnings

Marvel Spiderman Hand Sanitizer With Case by is a Otc medication manufactured, distributed, or labeled by Best Brand Consumers Products, Inc., Huizhou Bliss Commodity Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 68%

Purpose

Antiseptic

Use

To decrease the bacteria on the skin that could cause disease

Recommended for repeated use

Warnings

For external use only.

Flammable. Keep away from heat and flame

Discontinue if skin becomes irritated and ask a doctor

WHEN USING

Keep out of eyes. In case of contact with eyes, flush thoroughly with water

Do not inhale or ingest

Avoid contact with broken skin

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of accidental ingestion, seek professional assitance or contact a Poison Control Center immediately.

Directions

Wet hands thoroughly with products and rub untill dry withour wiping

For children under 6, use only under adult supervision

Not recommended for infants

Other information

Do not store above 105F

May discolor some fabrics

Harmful to wooden finishes and plastics

Inactive ingredients

Water, glycerin, propylene glycol, carbomer, sodium hydroxide, fragrance

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MARVEL SPIDERMAN HAND SANITIZER WITH CASE 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74530-044
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	68 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
CARBOMER 940 (UNII: 4Q93RCW27E)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74530-044-01	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/25/2020

Labeler - Best Brand Consumers Products, Inc. (058304494)

Establishment
Name	Address	ID/FEI	Business Operations
Huizhou Bliss Commodity Co., Ltd		417467331	manufacture(74530-044)