Search by Drug Name or NDC

NDC 73088-0204-11 HAND SANITIZER 62.5 g/100mL Details

HAND SANITIZER 62.5 g/100mL

HAND SANITIZER is a TOPICAL GEL in the HUMAN OTC DRUG category. It is labeled and distributed by TUBBY TODD. The primary component is ALCOHOL.

Product Information

NDC	73088-0204
Product ID	73088-204_da338eb7-32ec-654d-e053-2a95a90a25ac
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	HAND SANITIZER
Proprietary Name Suffix	COCONUT
Non-Proprietary Name	ALCOHOL
Product Type	HUMAN OTC DRUG
Dosage Form	GEL
Route	TOPICAL
Active Ingredient Strength	62.5
Active Ingredient Units	g/100mL
Substance Name	ALCOHOL
Labeler Name	TUBBY TODD
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part333A
Listing Certified Through	2023-12-31

Package

Package Images

NDC 73088-0204-11 (73088020411)

Pricing Information	N/A
NDC Package Code	73088-204-11
Billing NDC	73088020411
Package	59 mL in 1 BOTTLE (73088-204-11)
Marketing Start Date	2021-04-20
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL d2730c1d-a06c-4b68-9de3-676b3f23cbd8 Details

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.

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER COCONUT

alcohol gel

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

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

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

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

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	04/20/2021

Labeler - TUBBY TODD (052545299)

Revised: 3/2022

Document Id: da338eb7-32ec-654d-e053-2a95a90a25ac

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

Version: 5

Effective Time: 20220314