Lido AID by Diabetic Supply of Suncoast, Inc. Lido AID 0.17 oz (5mL)

Lido AID by

Drug Labeling and Warnings

Lido AID by is a Otc medication manufactured, distributed, or labeled by Diabetic Supply of Suncoast, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LIDO AID- lidocaine hcl gel 
Diabetic Supply of Suncoast, 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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Lido AID 0.17 oz (5mL)

DRUG FACTS

Active ingredient and Purpose

Active ingredientsPurpose
Lidocaine HCL 4%............................Topical analgesic

Uses

For the temporary relief of pain and itching.

Warnings

For external use only. Avoid contact with the eyes.

Do not use

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

Stop use and ask a doctor if

condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.

If pregnant or breast feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions

adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily

children under 2 years of age: consult a doctor

Other information

▪ store in a cool dry place between (59-86°F)15-30°C

▪ don’t use if seal over cap is broken, torn, or missing

Inactive ingredients

imidurea, methylparaben, menthol, propylene glycol, propylparaben, trolamine, water.

Questions or comments?

Toll-Free +1-888-373-2824 (24/7) www.advocatemeters.com

Distributed by:

Diabetic Supply of Suncoast, Inc
dba Advocate Diabetes.

PO Box 2102, Vega Alta, PR 00692

Principal Display Panel

Advocate

LidoAID

portable pain relieving

with LIDOCAINE HCL 4%

0.17 oz. (5 mL)

LidoAid PDP

LIDO AID 
lidocaine hcl gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 71814-120
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 mg  in 100 mg
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
IMIDUREA (UNII: M629807ATL)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
TROLAMINE (UNII: 9O3K93S3TK)  
MENTHOL (UNII: L7T10EIP3A)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 71814-120-051 in 1 BOX11/11/202001/01/2021
15 mg in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/21/201911/30/2022
Labeler - Diabetic Supply of Suncoast, Inc. (043081723)

Revised: 12/2022