DERMARITE ANTIBACTERIAL WET WIPES- alcohol cloth

DermaRite Antibacterial Wet Wipes by

Drug Labeling and Warnings

DermaRite Antibacterial Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Shaoxing Hengsheng New Material Technology Development Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 75%

antiseptic

USE

For hand sanitizing to decrease bacteria on the skin

Warning

For external use only
Do not use in or contact the eyes
This wipes are meant for general cleaning
This wipes do not rep lace wipes used for medical procedures
keep this out of reach of children.Store below 95 F(35 C)
If swallowed,get medical help or contract a Poison Control Center
immediately
Keep in a dry place away from fire
Discontinue use if irritation and redness develop.lf the condition
persists for more than 72 hours,consult a physician.
Please close the lid after dispensing to maintain purity Aicohol by
nature evaporates quickly.

Keep this out of reach of children

Directions

. Wet hands thoroughly with product and allow to dry without wiping.

Inactive ingredients

Purified Water,Glycerin,Aloe Barbadensis
extract,Phenoxyethanol,Ethylhexylglycerin,
Propylene Glycol.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DERMARITE ANTIBACTERIAL WET WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79770-001
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79770-001-01	10 in 1 BAG	07/20/2020
1		4.4 g in 1 NOT APPLICABLE; Type 0: Not a Combination Product
2	NDC: 79770-001-02	20 in 1 BAG	07/20/2020
2		4.4 g in 1 NOT APPLICABLE; Type 0: Not a Combination Product
3	NDC: 79770-001-03	30 in 1 BAG	07/20/2020
3		4.4 g in 1 NOT APPLICABLE; Type 0: Not a Combination Product
4	NDC: 79770-001-04	50 in 1 BAG	07/20/2020
4		4.4 g in 1 NOT APPLICABLE; Type 0: Not a Combination Product
5	NDC: 79770-001-05	80 in 1 BAG	07/20/2020
5		4.4 g in 1 NOT APPLICABLE; Type 0: Not a Combination Product
6	NDC: 79770-001-06	100 in 1 BAG	07/20/2020
6		4.4 g in 1 NOT APPLICABLE; Type 0: Not a Combination Product
7	NDC: 79770-001-07	110 in 1 PAIL	07/20/2020
7		4.4 g in 1 NOT APPLICABLE; Type 0: Not a Combination Product
8	NDC: 79770-001-08	160 in 1 PAIL	07/20/2020
8		4.4 g in 1 NOT APPLICABLE; Type 0: Not a Combination Product
9	NDC: 79770-001-09	400 in 1 PAIL	07/20/2020
9		4.4 g in 1 NOT APPLICABLE; Type 0: Not a Combination Product
10	NDC: 79770-001-10	800 in 1 PAIL	07/20/2020
10		4.4 g in 1 NOT APPLICABLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/20/2020

Labeler - Shaoxing Hengsheng New Material Technology Development Co., Ltd. (526871362)

Establishment
Name	Address	ID/FEI	Business Operations
Shaoxing Hengsheng New Material Technology Development Co., Ltd.		526871362	manufacture(79770-001)