SOLGREAT INSTANT HAND SANITIZER- ethyl alcohol gel

SolGreat Instant Hand Sanitizer by

Drug Labeling and Warnings

SolGreat Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by PANATURAL USA, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active lngredient  

Ethyl Alcohol

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.

Directions

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

Inactives 

aloe barbadensis leaf juice, carbomer, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, water.

Keep out of reach of children.

Children must be supervised in use of this product.

Other information

• store below 1100F (43oC).
• may discolor certain fabrics or surfaces.

Product Labe-60mL SolGreat Alcohol Hand Sanitizer

Product Label-237mL SolGreat Alcohol Hand Sanitizerr

Product Label 500mL SolGreat Alcohol Hand Sanitizer

INGREDIENTS AND APPEARANCE

SOLGREAT INSTANT HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73913-001
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
CARBOMER 1342 (UNII: 809Y72KV36)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73913-001-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/27/2020
2	NDC: 73913-001-02	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/27/2020
3	NDC: 73913-001-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/23/2020

Labeler - PANATURAL USA, INC. (029572239)