Wet Wipes by Anhui Germaphob Daily Commodity Co., Ltd. 80110-018 Wet Wipes

Wet Wipes by

Drug Labeling and Warnings

Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Anhui Germaphob Daily Commodity Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WET WIPES- wet wipes cloth 
Anhui Germaphob Daily Commodity Co., Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

80110-018
Wet Wipes

Active Ingredient(s)

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use only

Do not use in the eyes

Stop use and ask a doctor if
irritation and redness develop
condition persists for more than 72 hours

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

Do not use

Do not use in the eyes

When using this product Stop use and ask a doctor if
irritation and redness develop
condition persists for more than 72 hours

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

Stop use and ask a doctor if
irritation and redness develop
condition persists for more than 72 hours

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

Directions

wet hands thoroughly with product and allow to dry without wiping

Other information

/

Inactive ingredients

Water, glycerin, propylene glycol, EDTA disodium salt, phenoxyethanol, aloe vera leaf juice, tocopheryl acetate.

Package Label - Principal Display Panel

BAG80110-018-03 20PBAG80110-018-01 1PDRUM80110-018-20 800PDRUM80110-018-10 60P1BAG80110-018-02 10PBAG80110-018-06 80PBAG80110-018-04 40PBAG80110-018-08 120PDRUM80110-018-09 40PDRUM80110-018-11 80PDRUM80110-018-18 400PDRUM80110-018-13 120PBAG80110-018-05 50PDRUM80110-018-19 600PDRUM80110-018-14 160PDRUM80110-018-17 260PDRUM80110-018-16 250PDRUM80110-018-12 100PBAG80110-018-07 100PDRUM80110-018-15 200P

WET WIPES 
wet wipes cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 80110-018
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
WATER (UNII: 059QF0KO0R)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 80110-018-011 in 1 BAG; Type 0: Not a Combination Product09/16/2020
2NDC: 80110-018-07100 in 1 BAG; Type 0: Not a Combination Product09/16/2020
3NDC: 80110-018-0440 in 1 BAG; Type 0: Not a Combination Product09/16/2020
4NDC: 80110-018-0550 in 1 BAG; Type 0: Not a Combination Product09/16/2020
5NDC: 80110-018-08120 in 1 BAG; Type 0: Not a Combination Product09/16/2020
6NDC: 80110-018-0680 in 1 BAG; Type 0: Not a Combination Product09/16/2020
7NDC: 80110-018-0210 in 1 BAG; Type 0: Not a Combination Product09/16/2020
8NDC: 80110-018-0320 in 1 BAG; Type 0: Not a Combination Product09/16/2020
9NDC: 80110-018-0940 in 1 DRUM; Type 0: Not a Combination Product09/16/2020
10NDC: 80110-018-15200 in 1 DRUM; Type 0: Not a Combination Product09/16/2020
11NDC: 80110-018-16250 in 1 DRUM; Type 0: Not a Combination Product09/16/2020
12NDC: 80110-018-17260 in 1 DRUM; Type 0: Not a Combination Product09/16/2020
13NDC: 80110-018-18400 in 1 DRUM; Type 0: Not a Combination Product09/16/2020
14NDC: 80110-018-1060 in 1 DRUM; Type 0: Not a Combination Product09/16/2020
15NDC: 80110-018-19600 in 1 DRUM; Type 0: Not a Combination Product09/16/2020
16NDC: 80110-018-1180 in 1 DRUM; Type 0: Not a Combination Product09/16/2020
17NDC: 80110-018-14160 in 1 DRUM; Type 0: Not a Combination Product09/16/2020
18NDC: 80110-018-12100 in 1 DRUM; Type 0: Not a Combination Product09/16/2020
19NDC: 80110-018-20800 in 1 DRUM; Type 0: Not a Combination Product09/16/2020
20NDC: 80110-018-13120 in 1 DRUM; Type 0: Not a Combination Product09/16/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/16/202001/05/2022
Labeler - Anhui Germaphob Daily Commodity Co., Ltd. (554545209)
Establishment
NameAddressID/FEIBusiness Operations
Anhui Germaphob Daily Commodity Co., Ltd.554545209manufacture(80110-018)

Revised: 1/2022
Document Id: d4d2b928-3e34-1142-e053-2a95a90ad507
Set id: b201524e-055e-15d3-e053-2a95a90ad712
Version: 6
Effective Time: 20220105
 
A
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.