ALCOHOL liquid ALCOHOL gel

Alcohol by

Drug Labeling and Warnings

Alcohol by is a Otc medication manufactured, distributed, or labeled by Hello Bello, Unconditional Love. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol - 62.0%

PURPOSE

Antiseptic

USES:

For hand washing to decrease bacteria on skin

• Recommended for repeated use.

WARNINGS:

For external use only

• Flammable
• Keep away from fire/flame

• Do not use this product in or near eyes. If contact occurs rinse thoroughly with water

• Keep out of reach of children
• If swallowed, get medical help or contact a Poison Control Center right away
• Children under six years of age should be supervised.

DIRECTIONS:

Dispense an adequate amount in your palm to cover all surfaces of hands completely

• Rub hands together until dry
• Does not require rinsing.

OTHER INFORMATION:

Do not store above 104°F/40°C.

• May discolor some fabrics.

INACTIVE INGREDIENTS:

Aloe Barbadensis Leaf Juice. Calendula Officinalis Flower Extract Chamomilla Recutita (Matricaria) Flower Extract, Glycerin, Water

Principal Display Panel – 59 mL Bottle Label

hello
bello™

Fragrance-Free

Made with Aloe, Calendula,
and Chamomile Extracts.

+ Safe & effective for kids and adults
+ Vegan and cruelty-free
+ No sticky residue

Kills Germs

Hand Sanitizer
Spray

2.0 fl. oz. (59 ml) e

Principal Display Panel – 118 mL Bottle Label

Non-Sterile Solution

hello
bello™

Alcohol Antiseptic 80%
Topical Solution

Lavender

80% Alcohol

Hand Sanitizer
Spray

4 fl. oz. (118 ml) e

Principal Display Panel – 118 mL Bottle Label

Non-Sterile Solution

hello
bello™

Alcohol Antiseptic 80%
Topical Solution

80% Alcohol

Hand Sanitizer
Spray

4 fl. oz. (118 ml) e

Principal Display Panel – 236 mL Bottle Label

hello
bello™

Fragrance-Free

70% Alcohol

Hand Sanitizer Gel

8 fl. oz. (236 ml) e

INGREDIENTS AND APPEARANCE

ALCOHOL 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73418-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Calendula Officinalis Flower (UNII: P0M7O4Y7YD)
Chamomile (UNII: FGL3685T2X)
Glycerin (UNII: PDC6A3C0OX)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73418-030-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/01/2020

ALCOHOL 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73418-031
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
Hydrogen Peroxide (UNII: BBX060AN9V)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73418-031-01	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/01/2020

ALCOHOL 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73418-032
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
Hydrogen Peroxide (UNII: BBX060AN9V)
Water (UNII: 059QF0KO0R)
Lavender Oil (UNII: ZBP1YXW0H8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73418-032-01	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/01/2020

ALCOHOL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73418-033
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
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73418-033-01	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/01/2020

Labeler - Hello Bello (081135707)

Establishment
Name	Address	ID/FEI	Business Operations
Unconditional Love		081135707	MANUFACTURE(73418-030, 73418-031, 73418-032, 73418-033)