DermaFoam Premium Antibacterial
- Manufacturer
- Superior Chemical Corporation | Betco corporation, Ltd.
- Effective date
- 2024-11-20
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 7
- Source
- full-release
- Hydrated at
- 2026-06-01 00:48:29
Label at a glance#
ProductDermaFoam Premium Antibacterial
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredient
Triclosan 0.30%
INDICATIONS & USAGE SECTION
Uses
- Antibacterial hand cleaner.
- Use in a variet of public facilities including daycare centers, hospitals, nursing homes, physicians offices.
WARNINGS SECTION
Warnings
- For external use only.
- Avoid contact with eyes.
- Children under the age of 6 should be supervised by an adult when using this product.
- Discontinue use is irritation or redness develops.
- If irritation persists for more than 72 hours, consult a physician.
- KEEP OUT OF REACH OF CHILDREN.
DOSAGE & ADMINISTRATION SECTION
Directions
- Read the entire label before using this product.
- Dispense 0.8 mL of product onto wet palm.
- Rub hands together to distribute product, then rinse hands with clean.
INACTIVE INGREDIENT SECTION
Inactive Ingredients
Water, Potasium cocoate (contains coconut), Propylene Glycol, Glycerine, DMDM Hydantoin, Fragrance, FD&C Yellow #5, Aloe Barbadensis Leaf Juice. FD&C Red #40.
OTC - QUESTIONS SECTION
Questions or Comments?Phone: (800) 777-9343
MDS information:(800) 891-4965
OTC - PURPOSE SECTION
Purpose
Antibacterial
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1046593 | benzalkonium chloride 0.13 % Medicated Liquid Soap | PSN | 7 |
| 1046593 | benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap | SCD | 7 |
| 1046593 | benzalkonium chloride 0.13 % Medicated Liquid Soap | SY | 7 |
| 1046593 | benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap | SY | 7 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 5eb9f24b-9328-475e-af0a-18021935eb6a | Product name | 1 | 20180220 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53125-709-39 | DermaFoam Premium Antibacterial | 1000 mL in 1 BAG | SOAP | 1000 | 7 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- DermaFoam Premium Antibacterial
- Benzalkonium Chloride
- LIMONENE, (+)-
- WATER
- GLYCERIN
- FD&C YELLOW NO. 5
- METHYLCHLOROISOTHIAZOLINONE
- METHYLISOTHIAZOLINONE
- FD&C RED NO. 40
- BENZALKONIUM
- CITRAL
- 2-TERT-BUTYLCYCLOHEXYL ACETATE
- GERANIOL
- ALOE BARBADENSIS LEAF JUICE
- MAGNESIUM NITRATE
- ALLYL HEPTANOATE
- TETRASODIUM GLUTAMATE DIACETATE
- 2-TERT-BUTYLCYCLOHEXYLOXYBUTANOL
- 4-CYCLOHEXYL-2-METHYL-2-BUTANOL
- LINALOOL
- HYDROGEN PEROXIDE
- COCAMIDOPROPYLAMINE OXIDE
- ANHYDROUS CITRIC ACID
- 2,6-DIMETHYLOCTAN-2-OL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 53125-709 | 53125-709-39 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| 275c3182-2d79-7171-e063-6394a90a2f65 | 9a2fc005-5881-48c7-b2a3-3881ec88c2d1 | 2024-11-20 | Warnings | 275c3182-2d79-7171-e063-6394a90a2f65 9a2fc005-5881-48c7-b2a3-3881ec88c2d1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.