Tubby Todd (as PLD) - Hand Sanitizer (Coconut) (73088-204) - DELIST

HAND SANITIZER by

Drug Labeling and Warnings

HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by TUBBY TODD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER COCONUT- alcohol gel 
TUBBY TODD

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Tubby Todd (as PLD) - Hand Sanitizer (Coconut) (73088-204) - DELIST

ACTIVE INGREDIENTS

DENATURED DEHYDRATED ALCOHOL 40B  62.5%

PURPOSE

ANTISEPTIC

USES

For hand washing to decrease bacteria on skin.

WARNINGS

For external use only. Flammable. Keep away from sources of fire or flame.
When using this product do not use near eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if skin irritation develops.

Keep out of reach of children. If swallowed, seek medical advice or contact a Poison Control Center immediately.

DIRECTIONS

• Apply onto palm of hand.
• Cover hands with product by thoroughly rubbing and allow to air dry without wiping.
• Use undiluted.
• Supervise children under 6 years
• Not recommended for infants

OTHER INFORMATION

• Store below 86°F / 30°C
• Keep out of direct sunlight.

INACTIVE INGREDIENTS

WATER, GLYCERIN, PROPYLENE GLYCOL, CARBOMER, PROPANEDIOL, AMINOMETHYL PROPANOL, ALOE BARBADENSIS LEAF JUICE, TOCOPHERYL ACETATE (VITAMIN E ACETATE), HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, VACCINIUM MACROCARPON (CRANBERRY) FRUIT EXTRACT, PUNICA GRANATUM EXTRACT, VACCINIUM ANGUSTOFOLIA (BLUEBERRY) EXTRACT, FRAGARIA VESCA (STRAWBERRY) FRUIT EXTRACT, ACTINIDIA CHINENSIS (KIWI) EXTRACT

HAND SANITIZER  COCONUT
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73088-204
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	Â
GLYCERIN (UNII: PDC6A3C0OX)	Â
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	Â
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)	Â
PROPANEDIOL (UNII: 5965N8W85T)	Â
ALOE VERA LEAF (UNII: ZY81Z83H0X)	Â
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	Â
SUNFLOWER OIL (UNII: 3W1JG795YI)	Â
CRANBERRY (UNII: 0MVO31Q3QS)	Â
POMEGRANATE (UNII: 56687D1Z4D)	Â
BLUEBERRY (UNII: 253RUG1X1A)	Â
STRAWBERRY (UNII: 4J2TY8Y81V)	Â
KIWI FRUIT (UNII: 71ES77LGJC)	Â
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)	Â

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73088-204-11	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2021	12/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	04/20/2021	12/31/2023

Labeler - TUBBY TODD (052545299)

Revised: 3/2024

Document Id: 14abc586-4204-9a91-e063-6394a90a2511

34390-5

Set id: d2730c1d-a06c-4b68-9de3-676b3f23cbd8

Version: 7

Effective Time: 20240327

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