Coconut Foaming Hand Sanitizer With Natural Vitamin E and Almond Oil

Coconut Foaming Hand Sanitizer With Natural Vitamin E and Almond Oil by

Drug Labeling and Warnings

Coconut Foaming Hand Sanitizer With Natural Vitamin E and Almond Oil by is a Otc medication manufactured, distributed, or labeled by TJA Health LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

COCONUT FOAMING HAND SANITIZER WITH NATURAL VITAMIN E AND ALMOND OIL- benzalkonium chloride liquid 
TJA Health LLC

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Coconut Foaming Hand Sanitizer With Natural Vitamin E and Almond Oil

DRUG FACTS

ACTIVE INGREDIENT

Benzalkonium Chloride 0.12%

PURPOSE

Antimicrobial

USES

• For hand sanitizing to decrease bacteria on the skin
• Recommended for repeated use

WARNINGS

For external use only. Avoid contact with eyes. In case of eye contact, flush with water. Discontinue use if irritation or redness occurs.

Keep out of reach of children

2 years of age and younger. If swallowed, get help or contact a Poison Control Center right away.

DIRECTIONS

Apply to dry hands, rub together, & let dry.

INACTIVE INGREDIENTS

Purified water, surfactant, vitamin E(natural, d-alpha tocopherol), almond oil (natural), polysorbate 20, isopropyl alcohol USP, natural essential oil complex, natutal coconut scent.

Package Labeling:

COCONUT FOAMING HAND SANITIZER WITH NATURAL VITAMIN E AND ALMOND OIL 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57660-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.2 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
ALMOND OIL (UNII: 66YXD4DKO9)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
ACETAMIDOETHOXYETHANOL (UNII: LVX2APC4XR)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57660-004-01	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/01/2022	08/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	03/01/2022	08/01/2024

Labeler - TJA Health LLC (078799634)

Revised: 2/2025

Document Id: 2d3fe528-a52a-ca3a-e063-6394a90a8452

34390-5

Set id: ef421e7b-01ac-4ee6-b96f-a2fa476741b0

Version: 3

Effective Time: 20250203