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, 2024.

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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:53675-173
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (LIDOCAINE)	LIDOCAINE	5 mg in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description
1	NDC:53675-173-00	65 mL in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/25/2017

Labeler - Aruba Aloe Balm NV (855442273)

Establishment
Name	Address	ID/FEI	Operations
Aruba Aloe Balm NV		855442273	manufacture(53675-173)

Revised: 10/2017

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