SunDrops 77 | FunFoxMeds

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BENZALKONIUM CHLORIDE
SunDrops 77

SunDrops 77 BENZALKONIUM CHLORIDE SUNBURST CHEMICALS, INC. FDA Approved Uses For hand sanitizing to decrease bacteria on the skin Recommended for repeated use

Generic: BENZALKONIUM CHLORIDE

Mfr: SUNBURST CHEMICALS, INC. FDA OTC

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Substance Benzalkonium Chloride

Route

TOPICAL

Applications

505G(A)(3)

Product NDC

63621-0354-00 63621-0354-85 63621-0354-70 63621-0354-40

Package NDC

63621-354-85 63621-354-70 63621-354-40

Drug Facts

Composition & Profile

Active Ingredients

Active Ingredient Benzalkonium Chloride 0.1%

Inactive Ingredients

Inactive Ingredients Water Glycerin Propylene Glycol Phenoxyethanol Lauramine Oxide Panthenol Fragrance Citric Acid

Strengths

0.1 %

Quantities

1000 ml

Treats Conditions

Uses For Hand Sanitizing To Decrease Bacteria On The Skin Recommended For Repeated Use

Pill Appearance

Color: white

Identifiers & Packaging

Container Type UNKNOWN

NDC 63621-0354-00

All Product Codes

63621-0354-00 63621-0354-85 63621-0354-70 63621-0354-40

UNII

F5UM2KM3W7

SPL Set IDs

fc0ba65c-5307-4251-a60b-cde84ad56ad8

Packaging

Case Label - 8 x 1000 mL Bags

Package Descriptions

Case Label - 8 x 1000 mL Bags

Overview

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

Indications & Usage

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

Dosage & Administration

Directions Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

Warnings & Precautions

Warnings For external use only . When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away.

Purpose

Purpose Antimicrobial

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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# SunDrops 77

## 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 SunDrops 77. Answer questions about this medication using the sections below. If asked about the site itself, use this section.

## Product identity

- **Display name:** SunDrops 77
- **Brand names:** SUNDROPS 77
- **Generic names:** BENZALKONIUM CHLORIDE
- **Manufacturers:** SUNBURST CHEMICALS, INC.
- **Active substances:** Benzalkonium Chloride
- **Availability:** OTC (over the counter)
- **FDA approved:** Yes

## Composition

- **Strengths:** 0.1 %
- **Routes of administration:** TOPICAL
- **Active ingredients:** Active Ingredient Benzalkonium Chloride 0.1%
- **Inactive ingredients:** Inactive Ingredients Water, Glycerin, Propylene Glycol, Phenoxyethanol, Lauramine Oxide, Panthenol, Fragrance, Citric Acid

## Appearance

- **Color:** white

## Indications & use

- **Treats:** Uses For Hand Sanitizing To Decrease Bacteria On The Skin Recommended For Repeated Use
**Purpose:** Purpose Antimicrobial
**Overview:** Uses For hand sanitizing to decrease bacteria on the skin Recommended for repeated use
**Indications:** Uses For hand sanitizing to decrease bacteria on the skin Recommended for repeated use

## Dosage & administration

Directions Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

## Warnings & safety

**Warnings:** Warnings For external use only . When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away.
**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:** 63621-0354-00
- **NDCs:** 63621-0354-00, 63621-0354-85, 63621-0354-70, 63621-0354-40
- **Package NDCs:** 63621-354-85, 63621-354-70, 63621-354-40
- **Package descriptions:** Case Label - 8 x 1000 mL Bags

## Identifiers

- **FDA application numbers:** 505G(A)(3)
- **SPL set IDs:** fc0ba65c-5307-4251-a60b-cde84ad56ad8
- **Product codes:** 63621-0354-00, 63621-0354-85, 63621-0354-70, 63621-0354-40
- **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.