Aloe Gel by Commercial Beverage Concepts, LLC ALOE GEL- alcohol gel

Aloe Gel by

Drug Labeling and Warnings

Aloe Gel by is a Otc medication manufactured, distributed, or labeled by Commercial Beverage Concepts, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame. Do not ingest or inhale.

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Fragrance (Parfum), Glycerin, Isopropyl Myristate, Polyethylene Glycol/Acrylates Copolymer, Tocopheryl Acetate, Water

PRINCIPAL DISPLAY PANEL

945.35mL NDC: 75594-071-09

1.89L NDC: 75594-071-10

3.78L NDC: 75594-071-11

237mL NDC: 75594-071-01

354mL NDC: 75594-071-03

946mL NDC: 75594-071-04

1.89L NDC: 75594-071-05

3.78L NDC: 75594-071-06

208.198L NDC: 75594-071-07

354mL NDC: 75594-071-16

237mL NDC: 75594-071-17

59ml NDC: 75594-071-18

118ml NDC: 75594-071-19

237ml NDC: 75594-071-20

355ml NDC: 75594-071-21

473ml NDC: 75594-071-22

946ml NDC: 75594-071-23

1.89L NDC: 75594-071-24

3.78L NDC: 75594-071-25

INGREDIENTS AND APPEARANCE

ALOE GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75594-071(NDC:74221-004)
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
RAPIDGEL EZ1 (UNII: 33JH4A7R2K)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75594-071-09	0.94635 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
2	NDC: 75594-071-10	1.89 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
3	NDC: 75594-071-11	3.78 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
4	NDC: 75594-071-01	0.237 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
5	NDC: 75594-071-03	0.473 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
6	NDC: 75594-071-04	0.946 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
7	NDC: 75594-071-05	1.89 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
8	NDC: 75594-071-06	3.78 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
9	NDC: 75594-071-07	208.198 L in 1 DRUM; Type 0: Not a Combination Product	07/23/2020
10	NDC: 75594-071-16	0.354 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
11	NDC: 75594-071-17	0.237 L in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	07/23/2020
12	NDC: 75594-071-18	0.59 L in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	07/23/2020
13	NDC: 75594-071-19	0.118 L in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	07/23/2020
14	NDC: 75594-071-20	0.237 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
15	NDC: 75594-071-21	0.355 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
16	NDC: 75594-071-22	0.473 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
17	NDC: 75594-071-23	0.946 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
18	NDC: 75594-071-24	1.89 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
19	NDC: 75594-071-25	3.78 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/23/2020

Labeler - Commercial Beverage Concepts, LLC (080925174)

Establishment
Name	Address	ID/FEI	Business Operations
Commercial Beverage Concepts, LLC		080925174	pack(75594-071) , repack(75594-071) , label(75594-071) , relabel(75594-071)