SUAVE ANTIBACTERIAL HAND WASH SEA MINERALS AND ALOE VERA- liquid hand wash antibacterial liquid

Suave Antibacterial Hand Wash Sea Minerals and Aloe Vera by

Drug Labeling and Warnings

Suave Antibacterial Hand Wash Sea Minerals and Aloe Vera by is a Otc medication manufactured, distributed, or labeled by Suave Brands Co, LLC, Consumer Product Partners (CPP) (MO). Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient Benzalkonium Chloride

INACTIVE INGREDIENT

Inactive Ingredients Water (Aqua), Lauramine oxide, Cocamidopropyl Betaine, Lauramidopropylamine Oxide, Sodium Chloride, Glycerin, Lavandula Angustifolia (Lavender) Oil, Tocopheryl Acetate*, Sodium Benzoate, Fragrance (Parfum), Citric Acid, Tetrasodium EDTA, PEG-150 Distearate, Benzophenone-4, Sodium Hydroxide, Myristamidopropylamine Oxide, Hexyl Cinnamal, Blue 1 (CI 42090)

PURPOSE

Purpose anti-bacterial

INDICATIONS & USAGE

Use For handwashing to decrease bacteria on the skin.

KEEP OUT OF REACH OF CHILDREN

Warnings

• For external use only.
• When using this product avoid contact with eyes. In case of eye contact, rinse eyes thoroughly with water.
• Stop use and ask a doctor if irritation to redness develop.
• Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

WARNINGS

Warnings

• For external use only.
• When using this product avoid contact with eyes. In case of eye contact, rinse eyes thoroughly with water.
• Stop use and ask a doctor if irritation to redness develop.
• Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions Dispense, work into a lather on hands. Rinse clean.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SUAVE ANTIBACTERIAL HAND WASH SEA MINERALS AND ALOE VERA 
liquid hand wash antibacterial liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83711-407
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
TETRASODIUM EDTA (UNII: MP1J8420LU)
BENZOPHENONE-4 (UNII: 1W6L629B4K)
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
CITRIC ACID (UNII: 2968PHW8QP)
SODIUM BENZOATE (UNII: OJ245FE5EU)
WATER (UNII: 059QF0KO0R)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
HEXYL CINNAMAL (UNII: 7X6O37OK2I)
BLUE 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83711-407-12	355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/23/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	10/23/2025

Labeler - Suave Brands Co, LLC (118965468)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners (CPP) (MO)		119091520	manufacture(83711-407)