Dosage and administration
Place enough product on hands at 6 inch of distance. Rub the product on your hands to cover all surfaces. Rinse your hands with water and dry with a clean tissue.
MM Foaming
- Manufacturer
- Drima S. de R.L. de C.V.
- Effective date
- 2020-11-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:08:43
Label at a glance#
ProductMM Foaming
Active ingredientBENZALKONIUM CHLORIDE, ALCOHOL
Label structure13 sections
Label contents#
Full prescribing information#
Active Ingredient
Alcohol 37.16%. Purpose: Antiseptic
Benzalkonium Chloride 0.42% Purpose: Antiseptic.
ASK DOCTOR SECTION
If irritation or rash occurs. These may be signs of a serious condition.
Do not use section
In children less than 2 months of age
on open skin wounds
KEEP OUT OF REACH OF CHILDREN
If swallowed, get medical help or contact a Poison Control Center right away.
WHEN USING SECTION
When usign this product keep out of eyesm ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Purpose section
Antiseptic
Other information
Store between 15-30C (59-86F)
Avoid freezing and excesive heat above 40C (104F)
Warnings
Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. For external use only. Flammable. Keep away from heat or flame.
Inactive ingredient section
Cocamide DEA, glycerin, n-butane, propane, sodium nitrite, sodium lauryl sulfate and water.
Directions
Place enough product on hands at 6 inch of distance.
Rub the product on your hands to cover all surfaces.
Rinse your hands with water and dry with a clean tissue.
Use(s)
Hand wash to elp reduce bacteria that potentially can cause disease. This product is recommended for repeated use.
Stop use section
Stop use if irritation or rash occurs. These may be signs of a serious condition.
Package label - Principal display panel 510 mL
510 mL NDC: 77860-004-01
Products#
Every source-derived product name is available through these pages.
- MM Foaming
- Benzalkonium Chloride
- GLYCERIN
- SODIUM LAURETH-5 SULFATE
- BENZALKONIUM
- BUTANE
- PROPANE
- SODIUM NITRITE
- ALCOHOL
- COCO DIETHANOLAMIDE
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 77860-004 | 77860-004-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCERIN | PDC6A3C0OX | IACT |
| SODIUM LAURETH-5 SULFATE | 410Q7WN1BX | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| BUTANE | 6LV4FOR43R | IACT |
| PROPANE | T75W9911L6 | IACT |
| SODIUM NITRITE | M0KG633D4F | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| COCO DIETHANOLAMIDE | 92005F972D | IACT |
| WATER | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| d103b4ce-ae5c-9aeb-e053-2995a90a1158 | b34ed6c4-dca6-331f-e053-2995a90a4bd6 | 2021-11-17 | Warnings | b34ed6c4-dca6-331f-e053-2995a90a4bd6 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.