TOUCHLESS CARE CLEAR PROTECTANT- touchless care clear protectant spray 
Crawford Healthcare, Inc.

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.

----------

Touchless Care CLEAR PROTECTANT SPRAY

Active Ingredient

Dimethicone 20%

Purpose

Skin Protectant

Uses

Warnings

Do not use on deep puncture wounds, serious burns or animal bites. For external use only. When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

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

Keep out of reach of children

If swallowed, get medical help or contact a poison control center immediately.

Directions

Other Information

Store at 59 oF - 87 oF (15 oC - 30 oC)

Inactive Ingredients

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

SPL Unclassified Section

Distributed by: Crawford Healthcare, Inc. Doylestown, PA 18901

Touchless Care is a registered trademark of Crawford Woundcare Ltd.

© Crawford Healthcare Ltd., 2016

www.crawfordhealthcare.com/us

1-855-522-2211

Made in the USA

Package Label

Crawford Clear Label

TOUCHLESS CARE CLEAR PROTECTANT 
touchless care clear protectant spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69502-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE20 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
MINERAL OIL (UNII: T5L8T28FGP)  
CYCLOMETHICONE (UNII: NMQ347994Z)  
PETROLATUM (UNII: 4T6H12BN9U)  
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
LANOLIN (UNII: 7EV65EAW6H)  
HEXAMETHYLDISILOXANE (UNII: D7M4659BPU)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
CHOLECALCIFEROL (UNII: 1C6V77QF41)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69502-002-5746 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/09/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34705/09/2017
Labeler - Crawford Healthcare, Inc. (042813710)

Revised: 4/2017
Document Id: 4cfeabd3-38ec-40d9-e054-00144ff8d46c
Set id: 4cfeabd3-38eb-40d9-e054-00144ff8d46c
Version: 1
Effective Time: 20170412
 
Crawford Healthcare, Inc.