Laflare Santix Antibacterial Moisturizing Wipes by NAICO Drug Facts

Laflare Santix Antibacterial Moisturizing Wipes by

Drug Labeling and Warnings

Laflare Santix Antibacterial Moisturizing Wipes by is a Otc medication manufactured, distributed, or labeled by NAICO. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LAFLARE SANTIX ANTIBACTERIAL MOISTURIZING WIPES- benzalkonium chloride liquid 
NAICO

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Drug Facts

ACTIVE INGREDIENT

Benzalkonium Chloride 0.1%

INACTIVE INGREDIENTS

Water, Phenoxyethanol, Glycerin, Sodium Benzoate, Polysorbate 20, Disodium EDTA, Citric Acid, Tocopheryl Acetate, Macadamia Integrifolia/Tetraphylla Seed Oil, Anthemis Nobilis Flower Extract, Fragrance

PURPOSE

Antimicrobial

WARNINGS

For external use only.
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Do not use
in children less than 2 months of age
on open skin wounds
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When using this productkeep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctorif irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

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

Uses

Instant hand antimicrobial to decrease bacteria on the skin

Directions

■ Wet hands thoroughly with product and allow to dry without wiping

■ Do not flush

Other information

Storage in a cool, dry place, Avoid freezing and excessive heat above 40 ℃ (104 ℉)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LAFLARE SANTIX ANTIBACTERIAL MOISTURIZING WIPES 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75536-0005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75536-0005-1	81 g in 1 CONTAINER; Type 0: Not a Combination Product	05/01/2020	06/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	05/01/2020	06/30/2020

Labeler - NAICO (694725335)

Registrant - NAICO (694725335)

Establishment
Name	Address	ID/FEI	Business Operations
NAICO		694725335	manufacture(75536-0005)

Revised: 1/2025

Document Id: 2b055781-75c6-a401-e063-6394a90a0a4c

34390-5

Set id: 7b6f8f2f-c020-4ba6-85cb-d1f55f1169f9

Version: 2

Effective Time: 20250106