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CRC Sunscreen Towel CRC

Dosage form: cloth
Ingredients: HOMOSALATE 20g in 856mL, OCTINOXATE 75g in 856mL, OCTISALATE 40g in 856mL, OXYBENZONE 50g in 856mL
Labeler: CRC Industries, Inc.
NDC Code: 66348-4105

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.

Active Ingredient                                                                                                          Purpose

Homosalate (2%)..........................................................................................................Sunscreen

Octinoxate (7.5%).........................................................................................................Sunscreen

Octisalate (4%).............................................................................................................Sunscreen

Oxybenzone (5%)........................................................................................................Sunscreen

Uses

  • Provides high protection against sunburn.
  • Retains SPF after 80 minutes of sweating or activity in the water.

Warnings

For external use only.

Flammable.  Keep away from heat and flame when applying this product.

When using this product

  • Keep out of eyes.  Rinse with water to remove.

Stop use and ask a doctor

  • If rash or irritation develops and lasts.

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Unfold towel.
  • Apply evenly before sun exposure.
  • For children under 6 months, consult a doctor.
  • Reapply after towel drying, swimming or sweating.

Inactive Ingredients

Acrylates/Octylacrylamide Copolymer, Ethanol, Fragrance

CRC SUNSCREEN TOWEL  CRC
sunscreen towel cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66348-4105
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HOMOSALATE (SALICYLIC ACID) HOMOSALATE20 g  in 856 mL
OCTINOXATE (2-ETHYLHEXYL 4-PHENYLBENZOPHENONE-2'-CARBOXYLATE) OCTINOXATE75 g  in 856 mL
OCTISALATE (SALICYLIC ACID) OCTISALATE40 g  in 856 mL
OXYBENZONE (BENZOPHENONE) OXYBENZONE50 g  in 856 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL80.1 g  in 856 mL
Packaging
#Item CodePackage Description
1NDC:66348-4105-19 mL in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35203/01/2010
Labeler - CRC Industries, Inc. (069880029)
Registrant - ITW Dymon (103307604)
Establishment
NameAddressID/FEIOperations
ITW Dymon103307604manufacture

Revised: 03/2010
Document Id: 4ad5dd24-c826-4975-8682-8080fec442ad
Set id: 92b1bdbe-aa58-4394-8a91-3c43ab7835ea
Version: 2
Effective Time: 20100322
 
CRC Industries, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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