NATURAL SEAL ITCH RELIEF FOR KIDS- lidocaine spray 
Kericure 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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Natural Seal® ITCH RELIEF

DRUG FACTS

Active Ingredients:

Lidocaine 1%

Purpose:

Topical anesthetic

Uses:

For the temporary relief of pain and itch in minor cuts, burns, scrapes, skin irritations, insect bites, rashes and sunburn

Warnings:

For external use only. Avoid contact with eyes. Do not ingest.

Keep out of reach from children 2 years of age and younger.

Directions:

Shake well then apply firm spray. DO NOT RUB IN. Allow a thin, clear film to set. Barrier is thin, invisible once dry. Apply up to 3× a day for 7 days. Consult a doctor if condition worsens.

Inactive Ingredients:

Purified water, ethanol, acrylates copolymer, cellulose 

FOR KIDS!

Worry free first aid for kids

Soothing • Protective • Waterproof Seal

for Cuts, Scrapes, Rashes, Burns & Insect Bites

Made by Moms for Moms!

Questions? Contact us at info@kericure.com or visit www.KeriCure.com

MADE IN THE USA

KeriCure® 

Baltimore, MD 21229

Packaging

IMAGE

NATURAL SEAL ITCH RELIEF FOR KIDS 
lidocaine spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78280-712
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78280-712-1025 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product10/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34810/01/2020
Labeler - Kericure Inc. (966638681)

Revised: 11/2020
Document Id: beb6867d-20fd-4a42-b4bf-af98c5ca7c85
Set id: 31cc0c95-5864-4737-b085-8f58e00f4f05
Version: 1
Effective Time: 20201111
 
Kericure Inc.