SAFETY FIRST HAND SANITIZER 70% ETOH- ethyl alcohol gel

Safety First Hand Sanitizer 70% EtOH by

Drug Labeling and Warnings

Safety First Hand Sanitizer 70% EtOH by is a Otc medication manufactured, distributed, or labeled by LifeTech Pharma, LLC, LifeTech Pharma. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

This hand Sanitizer was manufactured according to the Federal Register 21 CFR 310, utilizing:

a. USP/FCC grade Ethyl alcohol 99%

b. Distilled/purified water

c. Hydroxypropylcellulose (as Vegetable Cellulose)

d. Glycerin USP/FCC grade

e. Limonene (as fragrance)

f. Aloe Vera extract

Active Ingredient(s)

Ethyl alcohol 70%

Purpose

Antiseptic, Hand Sanitizer

Uses

Decreases bacteria on skin.

Warnings

For external use only. Flammable, keep away from flames.

When using this product

When using this product keep out of eyes. In case of contact, flush eyes with water.

Stop use

Stop use and ask doctor if irritation and redness develop.

Keep out of reach

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Rub hands thoroughly with product and allow to dry.
For children under 6, use only under adult supervision.

Other Information

Store below 110ºF (43ºC).
May discolor certain fabrics or surfaces.

Inactive ingredients

Inactive ingredients Distilled Water,
Vegetable Cellulose,
Glycerin, Aloe Vera, Fragrance.

8 oz Packaging & Label - Principal Display Panel

8 FL Oz (236 mL) - NDC: 75270-532-08

16 oz Packaging & Label - Principal Display Panel

16 FL Oz ( 473 mL) - NDC: 75270-532-16

32 oz Packaging & Label - Principal Display Panel

32 FL Oz ( 946 mL) - NDC: 75270-532-32

128 oz Packaging & Label - Principal Display Panel

1 Gallon (3.78 L) 128 FL Oz - NDC: 75270-105-28

INGREDIENTS AND APPEARANCE

SAFETY FIRST HAND SANITIZER 70% ETOH 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75270-532
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70.7 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF POLYSACCHARIDES (UNII: W21O437517)	0.01 mL  in 100 mL
LIMONENE, (+)- (UNII: GFD7C86Q1W)	0.1 mL  in 100 mL
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)	0.01 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	28.5 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.7 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75270-532-08	236 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	07/01/2020
2	NDC: 75270-532-16	473 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	07/01/2020
3	NDC: 75270-532-32	946 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	07/01/2020
4	NDC: 75270-532-28	3780 mL in 1 JUG; Type 0: Not a Combination Product	07/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/01/2020

Labeler - LifeTech Pharma, LLC (057492812)

Registrant - LifeTech Pharma, LLC (057492812)

Establishment
Name	Address	ID/FEI	Business Operations
LifeTech Pharma		057492812	manufacture(75270-532)