MM Foaming by Drima S. de R.L. de C.V.

MM Foaming by

Drug Labeling and Warnings

MM Foaming by is a Otc medication manufactured, distributed, or labeled by Drima S. de R.L. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MM FOAMING- benzalkonium chloride aerosol, spray 
Drima S. de R.L. de C.V.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active Ingredient

Alcohol 44%. Purpose: Antiseptic

Benzalkonium Chloride 0.05% 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, fragrance, 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: 77860-003-01

MM FOAMING 
benzalkonium chloride aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77860-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.05 g  in 100 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	44 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
BUTANE (UNII: 6LV4FOR43R)
PROPANE (UNII: T75W9911L6)
SODIUM NITRITE (UNII: M0KG633D4F)
COCO DIETHANOLAMIDE (UNII: 92005F972D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77860-003-01	510 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/08/2020	11/16/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/08/2020	11/16/2021

Labeler - Drima S. de R.L. de C.V. (951577552)

Registrant - Drima S. de R.L. de C.V. (951577552)

Establishment
Name	Address	ID/FEI	Business Operations
Drima S. de R.L. de C.V.		951577552	manufacture(77860-003) , label(77860-003) , pack(77860-003)

Revised: 11/2021

Document Id: d103ac3e-c8db-4546-e053-2995a90aa0f5

34390-5

Set id: b12d1e25-aed0-1589-e053-2a95a90ac009

Version: 2

Effective Time: 20211117