MMM DIAPER RASH CREAM- zinc oxide gel cream

MMM Diaper Rash Cream by

Drug Labeling and Warnings

MMM Diaper Rash Cream by is a Otc medication manufactured, distributed, or labeled by Southern Sales & Services, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients Purpose

Zinc Oxide 5% Skin Protectant

PURPOSE

Helps treat and prevent diaper rash.

Protects chafed skin associated with diaper rash and helps protect from wetness.

WARNINGS

For external use only. When using this product avoid contact with eyes. Stop use and ask a doctor if

• Condition worsens.
• Symptoms last more than 7 days or clear up and occur again within a few days.

If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE

Change wet and soiled diapers promptly. Cleanse the affected area, and allow to dry. Apply cream liberally as often as necessary, with each change, especially at bedtime or anytime when exposure to wet diapers may be prolonged.

STOP USE

Stop use and ask a doctor if

Condition worsens.
Symptoms last more than 7 days or clear up and occur again within a few days.

DOSAGE & ADMINISTRATION

Change wet and soiled diapers promptly. Cleanse the affected area, and allow to dry. Apply cream liberally as often as necessary, with each change, especially at bedtime or anytime when exposure to wet diapers may be prolonged.

INACTIVE INGREDIENT

Purified Water, cyclotetrasiloxane , Isopropyl palmitate, Ethylhexyl palmitate, Glycerin, Cyclopentasiloxane, Polyglyceryl-4 Isostearate, Cetyl PEG/PPG-10/1 Dimethicone, Hexyl Laurate, Dimethicone, Tocopherol (Vitamin E), Zea Mays Oil, Retinyl palmitate(Vitamin A), Cholecalciferol (Vitamin D), Beeswax, Hydrogenated Castor Oil, Sodium Chloride, DMDM Hydantoin.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away

MMM Diaper Rash Cream

INGREDIENTS AND APPEARANCE

MMM DIAPER RASH CREAM 
zinc oxide gel cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69822-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CHOLECALCIFEROL (UNII: 1C6V77QF41)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
DIMETHICONE (UNII: 92RU3N3Y1O)
TOCOPHEROL (UNII: R0ZB2556P8)
HEXYL LAURATE (UNII: 4CG9F9W01Q)
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
WATER (UNII: 059QF0KO0R)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
GLYCERIN (UNII: PDC6A3C0OX)
MONOPHENYLHEPTAMETHYLCYCLOTETRASILOXANE (UNII: 50Q464790P)
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
YELLOW WAX (UNII: 2ZA36H0S2V)
DMDM HYDANTOIN (UNII: BYR0546TOW)
ETHYLHEXYL PALMITATE (UNII: 2865993309)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69822-007-60	170 g in 1 TUBE; Type 0: Not a Combination Product	01/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	01/01/2021

Labeler - Southern Sales & Services, Inc. (013114906)

Registrant - Southern Sales & Services, Inc. (013114906)