Dosage and administration
Pump a small amount of foam into palm of hand. Scrub thoroughly for at least fifteen seconds. Rinse completely and dry.
SunDrops 87
- Manufacturer
- Sunburst Chemicals, Inc.
- Effective date
- 2025-11-11
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 8
- Source
- full-release
- Hydrated at
- 2026-06-01 01:43:19
Label at a glance#
ProductSunDrops 87
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections
Label contents#
Full prescribing information#
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.
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
- 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
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Data code | Code 128 | 10784331199400 | SunDrops87C8.jpg |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63621-387-14 | SunDrops 87 | 3785 mL in 1 BOTTLE, PLASTIC | SOAP | 3785 | 8 | |
| 63621-387-40 | SunDrops 87 | 1000 mL in 1 BAG | SOAP | 1000 | 8 | |
| 63621-387-40 | SunDrops 87 | 4 in 1 BOX | SOAP | 4 | 8 | |
| 63621-387-50 | SunDrops 87 | 500 mL in 1 BOTTLE, PUMP | SOAP | 500 | 8 | |
| 63621-387-50 | SunDrops 87 | 6 in 1 BOX | SOAP | 6 | 8 | |
| 63621-387-65 | SunDrops 87 | 8 in 1 BOX | SOAP | 8 | 8 | |
| 63621-387-65 | SunDrops 87 | 1000 mL in 1 BAG | SOAP | 1000 | 8 |
Products#
Every source-derived product name is available through these pages.
- SunDrops 87
- Benzalkonium Chloride
- CITRIC ACID MONOHYDRATE
- BENZALKONIUM
- WATER
- GLYCERIN
- LAURAMINE OXIDE
- PEG-120 METHYL GLUCOSE DIOLEATE
- DMDM HYDANTOIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63621-387 | 63621-387-50, 63621-387-14, 63621-387-65, 63621-387-40 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| LAURAMINE OXIDE | 4F6FC4MI8W | IACT |
| PEG-120 METHYL GLUCOSE DIOLEATE | YM0K64F20V | IACT |
| DMDM HYDANTOIN | BYR0546TOW | IACT |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 7 | 2025-01-15 | full-release | 2026-06-01 00:52:53 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| SunDrops 87 | BENZALKONIUM CHLORIDE | Sunburst Chemicals, Inc. | 584ea129-aaf2-402f-b9f1-3fec2a23a21c | 2025-11-11 | Warnings | 63621-387-50 63621-387-65 63621-387-40 63621-387-14 63621-387 63621038765 63621038740 63621038750 63621038714 435389b8-9dde-0d17-e063-6294a90ab9b8 584ea129-aaf2-402f-b9f1-3fec2a23a21c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.