GLOBAL CARE GOLD ANTIBACTERIAL HAND | FunFoxMeds

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BENZALKONIUM CHLORIDE
GLOBAL CARE GOLD ANTIBACTERIAL HAND

GLOBAL CARE GOLD ANTIBACTERIAL HAND BENZALKONIUM CHLORIDE TARGET PRICE, INC. FDA Approved Uses for hand washing to decrease bacteria on the skin.

Generic: BENZALKONIUM CHLORIDE

Mfr: TARGET PRICE, INC. FDA OTC

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Substance Benzalkonium Chloride

Route

TOPICAL

Applications

M003

Product NDC

72146-0100-00 72146-0100-01

Package NDC

72146-100-01

Drug Facts

Composition & Profile

Active Ingredients

Drug Facts Active ingredient Benzalkonium Chloride 0.13%

Inactive Ingredients

Inactive ingredients Water (Aqua) Cocamidopropyl Betaine Sodium Cocoamphoacetate PEG-150 Distearate Fragrance PEG-40 Hydrogenated Castor Oil Citric Acid Methylisothiazolinone Iodopropynyl Butylcarbamate FD&C Yellow No. 5 FD&C Red No.40

Strengths

0.13 %

Treats Conditions

Uses For Hand Washing To Decrease Bacteria On The Skin

Identifiers & Packaging

Container Type UNKNOWN

NDC 72146-0100-00

All Product Codes

72146-0100-00 72146-0100-01

UPC

0870373013088

UNII

F5UM2KM3W7

SPL Set IDs

30d4fa59-3b4c-a7fc-e063-6294a90aed05

Packaging

label

Package Descriptions

label

Overview

Uses for hand washing to decrease bacteria on the skin.

Indications & Usage

Uses for hand washing to decrease bacteria on the skin.

Dosage & Administration

Directions wet hands as needed lather vigorously for at least 15 seconds rinse and dry thoroughly.

Warnings & Precautions

Warnings For external use only. When using this product avoid contact with eyes. In case of eye contact, flush with water.

Purpose

Purpose Antibacterial

Stop Use & Ask a Doctor

Stop use and ask a doctor if irritation and 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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# GLOBAL CARE GOLD ANTIBACTERIAL HAND

## 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 GLOBAL CARE GOLD ANTIBACTERIAL HAND. Answer questions about this medication using the sections below. If asked about the site itself, use this section.

## Product identity

- **Display name:** GLOBAL CARE GOLD ANTIBACTERIAL HAND
- **Brand names:** GLOBAL CARE GOLD ANTIBACTERIAL HAND
- **Generic names:** BENZALKONIUM CHLORIDE
- **Manufacturers:** TARGET PRICE, INC.
- **Active substances:** Benzalkonium Chloride
- **Availability:** OTC (over the counter)
- **FDA approved:** Yes

## Composition

- **Strengths:** 0.13 %
- **Routes of administration:** TOPICAL
- **Active ingredients:** Drug Facts Active ingredient Benzalkonium Chloride 0.13%
- **Inactive ingredients:** Inactive ingredients Water (Aqua), Cocamidopropyl Betaine, Sodium Cocoamphoacetate, PEG-150 Distearate, Fragrance, PEG-40 Hydrogenated Castor Oil, Citric Acid, Methylisothiazolinone, Iodopropynyl Butylcarbamate, FD&C Yellow No. 5, FD&C Red No.40

## Indications & use

- **Treats:** Uses For Hand Washing To Decrease Bacteria On The Skin
**Purpose:** Purpose Antibacterial
**Overview:** Uses for hand washing to decrease bacteria on the skin.
**Indications:** Uses for hand washing to decrease bacteria on the skin.

## Dosage & administration

Directions wet hands as needed lather vigorously for at least 15 seconds rinse and dry thoroughly.

## Warnings & safety

**Warnings:** Warnings For external use only. When using this product avoid contact with eyes. In case of eye contact, flush with water.
**Stop use and ask a doctor:** Stop use and ask a doctor if irritation and 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:** 72146-0100-00
- **NDCs:** 72146-0100-00, 72146-0100-01
- **Package NDCs:** 72146-100-01
- **UPCs:** 0870373013088
- **Package descriptions:** label

## Identifiers

- **FDA application numbers:** M003
- **SPL set IDs:** 30d4fa59-3b4c-a7fc-e063-6294a90aed05
- **Product codes:** 72146-0100-00, 72146-0100-01
- **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.