SunDrops 77

Manufacturer: Sunburst Chemicals, Inc.
Effective date: 2025-11-11
Label type: HUMAN OTC DRUG LABEL
Version: 9
Source: full-release
Hydrated at: 2026-06-01 01:43:22

Label at a glance#

ProductSunDrops 77

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Phenoxyethanol, Lauramine Oxide, Panthenol, Fragrance, Citric Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Case Label - 8 x 1000 mL Bags

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
63621-354-40	SunDrops 77	1000 mL in 1 BAG	SOAP	1000	9
63621-354-40	SunDrops 77	4 in 1 BOX	SOAP	4	9
63621-354-70	SunDrops 77	500 mL in 1 BOTTLE, PUMP	SOAP	500	9
63621-354-70	SunDrops 77	6 in 1 BOX	SOAP	6	9
63621-354-85	SunDrops 77	8 in 1 BOX	SOAP	8	9
63621-354-85	SunDrops 77	1000 mL in 1 BAG	SOAP	1000	9

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Benzalkonium Chloride	ACTIVE INGREDIENT	F5UM2KM3W7	2
Benzalkonium	ACTIVE MOIETY	7N6JUD5X6Y	2
CETRIMONIUM CHLORIDE	INACTIVE INGREDIENT	UC9PE95IBP	2
CITRIC ACID MONOHYDRATE	INACTIVE INGREDIENT	2968PHW8QP	2
DIHYDROXYETHYL COCAMINE OXIDE	INACTIVE INGREDIENT	8AR51R3BL5	2
GLYCERETH-17 COCOATE	INACTIVE INGREDIENT	3057VPT0KC	2
LAURTRIMONIUM CHLORIDE	INACTIVE INGREDIENT	A81MSI0FIC	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

SunDrops 77
Benzalkonium Chloride
PANTHENOL
PHENOXYETHANOL
CITRIC ACID MONOHYDRATE
WATER
BENZALKONIUM
PROPYLENE GLYCOL
LAURAMINE OXIDE
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63621-354	63621-354-85, 63621-354-70, 63621-354-40

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PANTHENOL	WV9CM0O67Z	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
PROPYLENE GLYCOL	6DC9Q167V3	IACT
LAURAMINE OXIDE	4F6FC4MI8W	IACT
GLYCERIN	PDC6A3C0OX	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
8	2024-10-15	full-release	2026-06-01 00:26:04

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Match
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SOAP / TOPICAL	0.5 %w/w	Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SOAP / TOPICAL	0.5 %w/w	Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SOAP / TOPICAL	0.5 %w/w	Exact identifier — unii+route+dosage form 4 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SOAP / TOPICAL	0.5 %w/w	Exact identifier — unii+route+dosage form 4 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SunDrops 77	BENZALKONIUM CHLORIDE	Sunburst Chemicals, Inc.	fc0ba65c-5307-4251-a60b-cde84ad56ad8	2025-11-11	Warnings	Exact identifier ndc (package): 63621-354-70 ndc (package): 63621-354-85 ndc (package): 63621-354-40 ndc (product): 63621-354 ndc11 (package): 63621035470 ndc11 (package): 63621035440 ndc11 (package): 63621035485 spl id: 43535ccc-3e06-c1e0-e063-6294a90a3acb spl set id: fc0ba65c-5307-4251-a60b-cde84ad56ad8

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.