SaniSmart 2
- Manufacturer
- Registered Chemicals Corporation
- Effective date
- 2018-03-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 22:54:55
Label at a glance#
ProductSaniSmart 2
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient
Benzalkonium Chloride 0.13%
OTC - PURPOSE SECTION
Purpose
Antimicrobial
INDICATIONS & USAGE SECTION
Uses •For hand washing to decrease bacteria on the skin
•Recommended for repeated use
WARNINGS SECTION
Warnings
For external use only.
When using this product avoid contact with eyes. In case of eye contact, flush eyes
thoroughly with water.
Stop use and ask a doctor if irritation or redness develop, 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.
DOSAGE & ADMINISTRATION SECTION
Directions •Pump a small amount of foam into palm of hand.
•Rub thoroughly over all surfaces of both hands for 15 seconds. •Rinse with potable water.
INACTIVE INGREDIENT SECTION
Inactive ingredients Water (Aqua), coco-glucoside, laurtrimonium chloride,
coamidopropylamine oxide, citric acid
OTC - QUESTIONS SECTION
Questions or comments? 781-803-7800 •info@registeredchemicals.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1046593 | benzalkonium chloride 0.13 % Medicated Liquid Soap | PSN | 2 |
| 1046593 | benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap | SCD | 2 |
| 1046593 | benzalkonium chloride 0.13 % Medicated Liquid Soap | SY | 2 |
| 1046593 | benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap | SY | 2 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72130-002-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-ed70-f424-e053-dadaa90a57ce | eb1d4d76-c2df-475a-98bb-541a5ea75769 |
| 72130-002-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-ed70-f424-e053-dadaa90a57ce | eb1d4d76-c2df-475a-98bb-541a5ea75769 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72130-002-01 | SaniSmart 2 | 3785 mL in 1 BOTTLE | LIQUID | 3785 | 2 | |
| 72130-002-02 | SaniSmart 2 | 1250 mL in 1 BOTTLE, SPRAY | LIQUID | 1250 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- SaniSmart 2
- BENZALKONIUM CHLORIDE
- BENZALKONIUM
- WATER
- COCO GLUCOSIDE
- LAURTRIMONIUM CHLORIDE
- COCAMIDOPROPYLAMINE OXIDE
- CITRIC ACID MONOHYDRATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72130-002 | 72130-002-02, 72130-002-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| COCO GLUCOSIDE | ICS790225B | IACT |
| LAURTRIMONIUM CHLORIDE | A81MSI0FIC | IACT |
| COCAMIDOPROPYLAMINE OXIDE | M4SL82J7HK | IACT |
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 82f7f192-d281-4036-9e51-4c3d7f569788 | eb1d4d76-c2df-475a-98bb-541a5ea75769 | 2018-03-14 | Warnings | 82f7f192-d281-4036-9e51-4c3d7f569788 eb1d4d76-c2df-475a-98bb-541a5ea75769 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.