SYMMETRY HAND SANITIZER- hand sanitizer gel 
Orlandi 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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Active Ingredient(s)

Ethyl alcohol 62% Purpose - Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

For hand washing to decrease bacteria on the skin that could casue disease

Warnings

For external use only

Flammable, keep away from fire or flame.

Do not use

in or near the eyes

Stop use and ask a doctor if

irritation and redness develop
condition persists for more than 72 hours

Keep out of reach of children.

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

Do not use

Keep out of reach of children. If swallowed, get medical help or contact a poison control center immediately.

For external use only. Do not use in the eyes.

Package Label - Principal Display Panel

label

Directions

Other information

Flammable, keep away from fire or flame.

Inactive ingredients

water (aqua), acrylate crosspolymer, glycerine, porpylene glycol, isopropyl myristate, fragrance (parfum), aminomethyl propanol, alor barnadensis juice, and tocopheryl acetate

Keep out of reach of children.

label

label

SYMMETRY HAND SANITIZER 
hand sanitizer gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68320-800
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 0.9 mL
Inactive Ingredients
Ingredient NameStrength
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
PROPYLENE (UNII: AUG1H506LY)  
GLYCERIN 1,3-DIMETHYL ETHER (UNII: A0JF0DT9XK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68320-800-021 in 1 BOX12/30/2020
1NDC:68320-800-010.9 mL in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A12/30/2020
Labeler - Orlandi Inc. (079801467)
Registrant - orlandi Inc (079801467)
Establishment
NameAddressID/FEIBusiness Operations
Buckeye International Inc.077132280manufacture(68320-800)
Establishment
NameAddressID/FEIBusiness Operations
Orlandi Inc079801467repack(68320-800) , relabel(68320-800)

Revised: 12/2020
Document Id: b636d4ab-3a92-fad1-e053-2a95a90af22f
Set id: a40cf6a3-acef-a701-e053-2995a90a7901
Version: 8
Effective Time: 20201211
 
Orlandi Inc.