SOLGREAT ETHYL ALCOHOL- ethyl alcohol liquid

SolGreat Ethyl Alcohol by

Drug Labeling and Warnings

SolGreat Ethyl Alcohol 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.

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.

KEEP OUT OF REACH OF CHILDREN

Other information

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

Inactive ingredient

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

Product labels

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOLGREAT ETHYL ALCOHOL 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73913-006
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73913-006-01	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/13/2020
2	NDC: 73913-006-02	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/13/2020
3	NDC: 73913-006-03	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/13/2020

Labeler - PANATURAL USA, INC. (029572239)

Establishment
Name	Address	ID/FEI	Business Operations
Hefei Yatai Daily-Use Chemical Industry Co., Ltd.		654641724	manufacture(73913-006)