b+free Hand Sanitizer Spray with Aloe Vera and Vitamin E

b free Hand Sanitizer with Aloe Vera and Vitamin E by

Drug Labeling and Warnings

b free Hand Sanitizer with Aloe Vera and Vitamin E by is a Otc medication manufactured, distributed, or labeled by b+free. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

B FREE HAND SANITIZER WITH ALOE VERA AND VITAMIN E- alcohol liquid 
b+free

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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b+free Hand Sanitizer Spray with Aloe Vera and Vitamin E

Drug Facts

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

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

Warnings

Flammable, keep away from fire/flame. For external use only

Do not use

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

When using this product

• do not get into eyes. In case of contact, rinse eyes thoroughly with water
• do not inhale or ingest.

Stop and ask doctor if

• irritation and redness develop
• condition persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• wet hands thoroughly with product and allow to dry without wiping
• supervise children under 6 years of age when using this product to avoid swallowing

Other information

• store between 15-30ºC (59-86ºF)
• avoid freezing and excessive heat above 40ºC (104ºF)
• may discolor certain fabrics or surfaces

Inactive ingredients

Water, Glycerin, Fragrance, Tocopheryl Acetate (VITAMIN E), Aloe Barbadensis Leaf Extract

Package Labeling:20 mL

Package Labeling:50 mL

Package Labeling:100 mL

B FREE HAND SANITIZER WITH ALOE VERA AND VITAMIN E 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 90120-002
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)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 90120-002-01	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020	07/01/2023
2	NDC: 90120-002-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020	07/01/2023
3	NDC: 90120-002-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020	07/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/01/2020	07/01/2023

Labeler - b+free (013549109)

Revised: 9/2022

Document Id: e894a3c5-2e66-729d-e053-2995a90a7c87

34390-5

Set id: ae6bd776-8d84-1a13-e053-2a95a90a3e2e

Version: 4

Effective Time: 20220913