ECLADO ANTISEPTIC MOISTURE- alcohol spray 
Laon Cosmetic

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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ACTIVE INGREDIENT

Active ingredients: 60%

INACTIVE INGREDIENT

Inactive ingredients:

Water, Glycerin, Sodium Citrate, Glycereth-25 PCA Isostearate, Mentha Piperita (Peppermint) Oil, Lavandula Hybrida Herb Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil

PURPOSE

Purpose: ANTISEPTIC

WARNINGS

Warnings:

For external use only. Flammable. Keep away from heat or flame
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Do not use
• in children less than 2 months of age
• on open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Uses:

Hand and body antiseptic intended for preventing infectious diseases.

Directions

Directions:

• Spay enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

Other Information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

ECLADO ANTISEPTIC MOISTURE 
alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76900-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL102 mL  in 170 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Sodium Citrate (UNII: 1Q73Q2JULR)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
TEA TREE OIL (UNII: VIF565UC2G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76900-010-021 in 1 CARTON05/01/2020
1NDC:76900-010-01170 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/01/2020
Labeler - Laon Cosmetic (689201314)
Registrant - Laon Cosmetic (689201314)
Establishment
NameAddressID/FEIBusiness Operations
DASOL CO.,LTD.557839013manufacture(76900-010)

Revised: 5/2020
Document Id: 67f73583-ed39-405f-aa31-2094d7b76d75
Set id: c58c9c91-3275-45ba-b6f4-cd8f66351c85
Version: 1
Effective Time: 20200506
 
Laon Cosmetic