Active Ingredient(s)

Ethanol 75%

Purpose

Antiseptic

Use

Hand sanitizer to help reduce bacteria that potentially can cause disease

For use when soap and water are not available

Warnings

For external use only -hands

Highly flammable. Keep away from fire or flame

Avoid eyes. In case of eye contact, flush with water

Discontinue if skin irritation occurs. If condition persists, please consult a doctor.

Keep out of reach of children.

Directions

Squeeze 1/2 tea spoon amount in you plam then briskly rub hands together thoroughly until dry

Other information

Store below 104F (40C)

Inactive ingredients

Water, glycerol, aloe extract

image description

DALIS HAND SANITIZER
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:77639-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
GLYCEROL FORMAL (UNII: 3L7GR2604E)
WATER (UNII: 059QF0KO0R)
ALOE (UNII: V5VD430YW9)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:77639-001-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
2	NDC:77639-001-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
3	NDC:77639-001-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
4	NDC:77639-001-04	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
5	NDC:77639-001-05	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
6	NDC:77639-001-06	150 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
7	NDC:77639-001-07	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
8	NDC:77639-001-08	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
9	NDC:77639-001-09	280 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
10	NDC:77639-001-10	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
11	NDC:77639-001-11	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
12	NDC:77639-001-12	380 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
13	NDC:77639-001-13	400 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
14	NDC:77639-001-14	450 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
15	NDC:77639-001-15	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
16	NDC:77639-001-16	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
17	NDC:77639-001-17	600 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
18	NDC:77639-001-18	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
19	NDC:77639-001-19	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
20	NDC:77639-001-20	2500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
21	NDC:77639-001-21	3800 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
22	NDC:77639-001-22	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
23	NDC:77639-001-23	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
24	NDC:77639-001-24	20000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
25	NDC:77639-001-25	25000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
26	NDC:77639-001-26	50000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
27	NDC:77639-001-27	120000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020
28	NDC:77639-001-28	1000000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	05/12/2020

Labeler - Zhejiang Yongjin Biotechnology Co., Ltd (542189693)

Name	Address	ID/FEI	Business Operations
Establishment
Zhejiang Yongjin Biotechnology Co., Ltd		542189693	manufacture(77639-001)