HAND SANITIZER 29ML 01- alcohol liquid 
Shenzhen Lantern Scicence Co.,Ltd.

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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Hand sanitizer 29ml

Drug Facts

drug factsDrug Facts

Active Ingredient

Active Ingredient Purpose

Ethyl Alcohol 65%(V/V) Antiseptic

Use

Hand sanitizer helps to reduce bacteria that potentially can cause disease.For use when soap and water are not available.

Use(s)

To decrease bacteria on the skin that could cause disease.Recommended for repeated use.

Warning

For external use only-hands

Flammable.Keep away from heat and flame.

For external use only.

Flammable, keep away from heat and flame.

Discontinue if skin becomes irritated and ask a doctor .

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a poson control center immediately.

keep out of reach of children

In case of accidental ingestion,seek professional assistant or contact a Poison Control Center immediately.

Recommended for repeated use.

use anywhere without water.

Inactive ingredients

Water(Aqua), Fragrance,Carbomer,CI 42090,CI 16255.

Directions

Wet hands thoroughly with product and rub until dry without wiping.Children under 6,use only with adult supervision.

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Do not inhale or ingest.

Avoid contact with broken skin.

Other information

Do not store above 105F.

May discolor some fabrics.

Harmful to wood finishes and plastics.

When using this product

Do not use in or near eyes,In case of eye contact ,flush eyes thoroughly with water. Discontinue if skin becomes irritated and ask for a doctor.

Other information

store below 105℉

May discolor some fabrics and surfaces.

Purpose

Antiseptic

Packaging

PackagingPackaging

HAND SANITIZER 29ML  01
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54860-413
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R) 34.7397 mL  in 100 mL
CARBOMER 940 (UNII: 4Q93RCW27E) 0.26 mL  in 100 mL
FD&C RED NO. 4 (UNII: X3W0AM1JLX) 0.0002 mL  in 100 mL
FD&C BLUE NO. 1 (UNII: H3R47K3TBD) 0.0001 mL  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54860-413-0129 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/23/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/23/2023
Labeler - Shenzhen Lantern Scicence Co.,Ltd. (421222423)
Registrant - Lantern Beauty America,INC. (117371139)
Establishment
NameAddressID/FEIBusiness Operations
Shenzhen Lantern Science Co.,Ltd.421222423manufacture(54860-413)

Revised: 5/2023
Document Id: fc546a9f-63a7-39a3-e053-6294a90afc69
Set id: fc546a9c-a58a-7edf-e053-6394a90a7c21
Version: 32
Effective Time: 20230522
 
Shenzhen Lantern Scicence Co.,Ltd.