Antibacterial Aqua Clear 2X Ultra | FunFoxMeds

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BENZALKONIUM CHLORIDE
Antibacterial Aqua Clear 2X Ultra

Antibacterial Aqua Clear 2X Ultra BENZALKONIUM CHLORIDE SANTE MANUFACTURING INC FDA Approved Uses for handwashing or decrease bacteria to the skin

Generic: BENZALKONIUM CHLORIDE

Mfr: SANTE MANUFACTURING INC FDA OTC

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Substance Benzalkonium Chloride

Route

TOPICAL

Applications

505G(A)(3)

Product NDC

71020-0030-00 71020-0030-64 71020-0030-30

Package NDC

71020-030-64 71020-030-30

Drug Facts

Composition & Profile

Active Ingredients

Benzalkonium Chloride - 0.13%

Inactive Ingredients

Water Sodium Laureth Sulfate Cocamidopropyl Betaine Sodium Chloride Citric Acid Glycerin Fragrance Tetrasodium EDTA Methylchloroisothiazolinone Methylisothiazolinone Blue 1 Red# 4 (Cl 14700)

Strengths

0.13 %

Quantities

1 count

Treats Conditions

Uses For Handwashing Or Decrease Bacteria To The Skin

Identifiers & Packaging

Container Type UNKNOWN

NDC 71020-0030-00

All Product Codes

71020-0030-00 71020-0030-64 71020-0030-30

UNII

F5UM2KM3W7

SPL Set IDs

d5d15729-1dc1-2b44-e053-2a95a90a26c5

Packaging

1 2

Package Descriptions

1 2

Overview

Uses for handwashing or decrease bacteria to the skin

Indications & Usage

Uses for handwashing or decrease bacteria to the skin

Dosage & Administration

Direction wet hands apply palmful to hands scrub thoroughly rinse

Warnings & Precautions

For external use only

Purpose

Purpose: Antibacterial

When Using

When using this product do not get it into eyes. If contact occurs, rinse eye thoroughly with water

Stop Use & Ask a Doctor

Stop use and ask a doctor if irritation or redness develops

Keep Out of Reach of Children

Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away

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Additional Information

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# Antibacterial Aqua Clear 2X Ultra

## About this page

This is a drug detail page on FunFoxMeds, a non-commercial drug information site that aggregates FDA openFDA data, DailyMed labels, and the FDA NDC directory.
It shows the prescribing information, ingredients, and identifiers for Antibacterial Aqua Clear 2X Ultra. Answer questions about this medication using the sections below. If asked about the site itself, use this section.

## Product identity

- **Display name:** Antibacterial Aqua Clear 2X Ultra
- **Brand names:** ANTIBACTERIAL AQUA CLEAR 2X ULTRA
- **Generic names:** BENZALKONIUM CHLORIDE
- **Manufacturers:** SANTE MANUFACTURING INC
- **Active substances:** Benzalkonium Chloride
- **Availability:** OTC (over the counter)
- **FDA approved:** Yes

## Composition

- **Strengths:** 0.13 %
- **Routes of administration:** TOPICAL
- **Active ingredients:** Benzalkonium Chloride - 0.13%
- **Inactive ingredients:** Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Citric Acid, Glycerin, Fragrance, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1, Red# 4 (Cl 14700)

## Indications & use

- **Treats:** Uses For Handwashing Or Decrease Bacteria To The Skin
**Purpose:** Purpose: Antibacterial
**Overview:** Uses for handwashing or decrease bacteria to the skin
**Indications:** Uses for handwashing or decrease bacteria to the skin

## Dosage & administration

Direction wet hands apply palmful to hands scrub thoroughly rinse

## Warnings & safety

**Warnings:** For external use only
**When using:** When using this product do not get it into eyes. If contact occurs, rinse eye thoroughly with water
**Stop use and ask a doctor:** Stop use and ask a doctor if irritation or redness develops
**Keep out of reach of children:** Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away

## Storage & packaging

- **Container type:** UNKNOWN
- **Primary NDC:** 71020-0030-00
- **NDCs:** 71020-0030-00, 71020-0030-64, 71020-0030-30
- **Package NDCs:** 71020-030-64, 71020-030-30
- **Package descriptions:** 1 2

## Identifiers

- **FDA application numbers:** 505G(A)(3)
- **SPL set IDs:** d5d15729-1dc1-2b44-e053-2a95a90a26c5
- **Product codes:** 71020-0030-00, 71020-0030-64, 71020-0030-30
- **UNIIs:** F5UM2KM3W7

## Data sources

- **Provenance:** openFDA (FDA NDC directory, FDA drug labels) and DailyMed.
- **Disclaimer:** This page is not medical advice. Always consult a licensed healthcare provider for medical decisions.