Skip to main content

Alcoholada Gel Pain Relieving Pain

Dosage form: gel
Ingredients: LIDOCAINE HYDROCHLORIDE 5mg in 1mL
Labeler: Aruba Aloe Balm NV
NDC code: 53675-173

Medically reviewed by Drugs.com. Last updated on Oct 16, 2023.

Alcoholada Gel Pain Relieving Pain

Drug Facts

Active ingredient

Lidocaine Hydrochloride 0.5%

Purpose

Pain Relieving Gel

Uses

For the temporary relief of pain and itching associated with minor burns, sunburn, insect bites, or minor skin irritations.

Warnings

For external use only.

Do not use 

in large quantites, particularly over raw surfaces or blistered areas.

When using this product 

avoid contact with the eyes.

Stop use and ask a doctor if

conditions worsens, or if symptoms persist for more than 7 days or clears up nand occur again within a few days.

Keep out of reach of children.

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

Directions
  • Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
  • Children under2 years of age: Consult a doctor.

Other Information
  • Store in a cool dry place
  • Protect from heat and light

Inactive ingredients

Water (Aqua/Eau), Alcohol Denat. Polysorbate 20, Acrylates/C10-30 Alkyl Acrylate crosspolymer, Aloe Barbadensis Leaf Juice (Aloe Vera Gel from Aruba), Phenoxyethanol, Caprylyl Glycol, Chlorphenesin, Sodium Hydroxide, FD&C #1 (C.I. 42090), Fragrance (Parfum)

Package Labeling:

ALCOHOLADA GEL PAIN RELIEVING PAIN 
lidocaine hydrochloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53675-173
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ALCOHOL 
POLYSORBATE 20 
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) 
ALOE VERA LEAF 
PHENOXYETHANOL 
CAPRYLYL GLYCOL 
CHLORPHENESIN 
SODIUM HYDROXIDE 
FD&C BLUE NO. 1 
Packaging
#Item CodePackage Description
1NDC:53675-173-0065 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34810/25/2017
Labeler - Aruba Aloe Balm NV (855442273)
Establishment
NameAddressID/FEIOperations
Aruba Aloe Balm NV855442273manufacture(53675-173)

Document Id: 5c777635-df09-6955-e053-2a91aa0a3aee
Set id: b8c662dd-4af0-426b-b521-0a821868c888
Version: 1
Effective Time: 20171026
 
Aruba Aloe Balm NV

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer