SUNDROPS 87- benzalkonium chloride soap

SunDrops 87 by

Drug Labeling and Warnings

SunDrops 87 by is a Otc medication manufactured, distributed, or labeled by Sunburst Chemicals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Skin Antimicrobial

Use

Reduces amount of bacteria on hands

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.

Directions

• Pump a small amount of foam into palm of hand.
• Scrub thoroughly for at least fifteen seconds.
• Rinse completely and dry.

Inactive Ingredients

Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glycose Dioleate, DMDM Hydantoin, Citric Acid, Fragrance

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SUNDROPS 87 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63621-387
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
DMDM HYDANTOIN (UNII: BYR0546TOW)

Product Characteristics
Color	white (colorless - water-white, dispensed as a white foam)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63621-387-50	6 in 1 BOX	06/08/2020
1		500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 63621-387-14	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/2020	11/17/2023
3	NDC: 63621-387-65	8 in 1 BOX	07/14/2020
3		1000 mL in 1 BAG; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/08/2020

Labeler - Sunburst Chemicals, Inc. (006159339)