DE LA CRUZ CAMPHORATED ALCOHOL - camphor (synthetic) liquid 
DLC Laboratories, 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.

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De La Cruz Camphorated Alcohol

Active Ingredient

Camphor USP 11%

Purpose

External pain reliever

Uses

relieves minor aches

relieves minor pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.

Warnings

For external use only

When using this product

avoid contact with eyes

do not apply to wounds or damaged skin

do not bandage tightly

do not apply to irritated skin or mucous membranes

Stop use and consult a doctor if

condition worsens or if symptoms persist for more than 7 days

symptoms clear up and occur again with in a few days.

Keep out of the reach of children.

NOT TO BE TAKEN BY MOUTH.

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

Do not accept if seal around cap is broken or missing.

Directions

Adults and children 2 years of age or older, apply to affected area not more than 3 or 4 times daily.

children under 2 years of age: consult a doctor.

Inactive Ingredients:

isopropyl alcohol, purified water

Questions?

1-800-858-3889

De La Cruz

Alcohol Alcanforado

Analgeisco Externo



CAMPHORATED ALCOHOL
External Pain Reliever


8fl oz (236ml)

DLC Camphorated Alcohol

DE LA CRUZ CAMPHORATED ALCOHOL 
camphor liquid
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:24286-1527
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (CAMPHOR (SYNTHETIC)) CAMPHOR (SYNTHETIC)110 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ISOPROPYL ALCOHOL 
WATER 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24286-1527-259 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/15/2011
Labeler - DLC Laboratories, Inc. (093351930)

Revised: 3/2013
Document Id: bf13de44-3569-45a2-ba21-8e4f56510798
Set id: c75559e0-f2af-41cd-ac11-8f8e4fbc4a7a
Version: 7
Effective Time: 20130325
 
DLC Laboratories, Inc.