PANROSA INSTANT HAND SANITIZER ALOE VERA- alcohol gel

Panrosa Instant Hand Sanitizer Aloe Vera by

Drug Labeling and Warnings

Panrosa Instant Hand Sanitizer Aloe Vera by is a Otc medication manufactured, distributed, or labeled by Panrosa Enterprises, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

• hand sanitizer to help decrease bacteria on the skin, when water, soap & towel are not available.
• recommended for repeated use.

Warnings

For external use only. Flammable. Keep away from fire or flame.

Do not apply around eyes.

Do not use

in ears & mouth.

When using this product,

avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if

redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

Children must be supervised in use of this product.

Directions

• place enough product into your palms and thoroughly spread on both hands.
• rub into skin until dry.

Other information

• store below 110 ℉ (43℃ ). 
• may discolor certain fabrics or surfaces.

Inactive ingredients

water, carbomer, triethanolamine, glycerin, propylene glycol, fragrance, aloe barbadensis leaf juice, tocopheryl acetate, FD&C blue No. 1, FD&C yellow No. 5.

Package Labeling:50302-013-10

Package Labeling:50302-013-60

INGREDIENTS AND APPEARANCE

PANROSA INSTANT HAND SANITIZER ALOE VERA 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50302-013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50302-013-10	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/06/2020
2	NDC: 50302-013-60	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/06/2020

Labeler - Panrosa Enterprises, Inc. (859957578)