RASH RELIEF SILVER- dimethicone zinc oxide liquid

Rash Relief Silver by

Drug Labeling and Warnings

Rash Relief Silver by is a Otc medication manufactured, distributed, or labeled by Touchless Care Concepts LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Dimethicone             20%       

Petrolatum               25%

Silver                      25 ppm

Purpose

Skin Protectant.

Warnings

- For external use only.

- When using this product do not get into eyes.  If contact occurs, rinse eyes thoroughly with water.  For external use only. 

- Stop use and ask a doctor if condition worsens or does not improve in 7 days.

Directions

- Cleanse the skin area thoroughly. 

- Shake bottle well before use.

- Spray 4-6 inches from skin using firm/quick trigger motion. No rub-in is required.  Coating slowly dries over time.

- Reapply 1-3 times per day or as directed by health professional.

Inactive Ingredients

Cyclomethicone, Hexamethyldisiloxane, Lanolin, Light Mineral Oil, Microcrystalline Wax, Protein, Vitamin A Palmitate, Vitamin D3, Water, White Petrolatum

INDICATIONS & USAGE

Manage moisture, friction, and inflammation: skin folds, incontinence dermatitis, venous stasis/pressure ulcers, wounds

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.  If swallowed, get medical help or contact a local poison control center immediately.

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

RASH RELIEF SILVER  
dimethicone zinc oxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 15071-652
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Dimethicone (UNII: 92RU3N3Y1O) (Dimethicone - UNII:92RU3N3Y1O)	Dimethicone	20 g  in 100 g
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z)	Zinc Oxide	25 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
Mineral Oil (UNII: T5L8T28FGP)
Cyclomethicone (UNII: NMQ347994Z)
Lanolin (UNII: 7EV65EAW6H)
Microcrystalline Wax (UNII: XOF597Q3KY)
Hexamethyldisiloxane (UNII: D7M4659BPU)
Water (UNII: 059QF0KO0R)
Cholecalciferol (UNII: 1C6V77QF41)
Vitamin A Palmitate (UNII: 1D1K0N0VVC)
Petrolatum (UNII: 4T6H12BN9U)
Casein (UNII: 48268V50D5)
Silver (UNII: 3M4G523W1G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 15071-652-11	56 g in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	11/01/2008

Labeler - Touchless Care Concepts LLC (083459334)

Registrant - Touchless Care Concepts LLC (083459334)