FZ2161TA special ( clear, ocean breeze)

Ocean breeze scented hand sanitizer by

Drug Labeling and Warnings

Ocean breeze scented hand sanitizer by is a Otc medication manufactured, distributed, or labeled by Townley Inc., Jinhua Magic Color Cosmetic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

OCEAN BREEZE SCENTED HAND SANITIZER 01- alochol gel 
Townley 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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FZ2161TA special ( clear, ocean breeze)

Drug facts

Active ingredient .............purpose

alcohol Denate: 70%(v/v)..... Antibacterial

Use

To decrease bacteria on the skin that could cause disease.

Warnings

For external use only-hands

keep out of eyes- avoid contact with broken skin.

Keep away from fire.

Stop use and ask a dosctor if irritation or radness develops

Do not inhale or ingest. If swallowed, get medical help or contact a poison control right away.

Direction

Rub a dime sized drop into hands.

For children under 8 use under adult supervision

Inactive ingredients

INACTIVE INGREDIENTS: WATER(AQUA/EAU), PEG-40 HYDROGENATED CASTOR OIL, FRAGRANCE( PARFUM), ACRYLATES/ c10-30 ALKYL ACRYLATE CROSSPOLYMER, TRIETHANOLAMINE.

Questions?

1-212-779-0544 weekdays

72005-102-01

OCEAN BREEZE SCENTED HAND SANITIZER  01
alochol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 72005-102
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
TROLAMINE (UNII: 9O3K93S3TK) 0.16 g  in 100 mL
WATER (UNII: 059QF0KO0R) 37.2397 g  in 100 mL
HOLODISCUS DISCOLOR WHOLE (UNII: 2AVP26HMCJ) 0.2 g  in 100 mL
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) 0.2 mL  in 100 mL
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) 0.2 mL  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 72005-102-01236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/26/202004/20/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/26/202004/20/2021
Labeler - Townley Inc. (016956158)
Registrant - Townley Inc. (016956158)
Establishment
NameAddressID/FEIBusiness Operations
Townley Inc.016956158label(72005-102)
Establishment
NameAddressID/FEIBusiness Operations
Jinhua Magic Color Cosmetic Co., Ltd.529434788manufacture(72005-102)

Revised: 4/2021
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