MEDICALLY MINDED- benzalkonium chloride cloth

MEDICALLY MINDED by

Drug Labeling and Warnings

MEDICALLY MINDED by is a Otc medication manufactured, distributed, or labeled by BELSKIN S. DE, R.L. DE C.V. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE AND ADMINISTRATION

APPLY TO HANDS

ALLOW TO DRY WITHOUT WIPING

WARNINGS AND PRECAUTIONS

WHEN USING THIS PRODUCT DO NOT GET INTO EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.

CHILDREN UNDER 2 YEARS ASK A DOCTOR BEFORE USE

WARNINGS

FOR EXTERNAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

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

STOP USE AND ASK A DOCTOR IF IRRITATION OR RASH DEVELOPS AND CONTINUES FOR MORE THAN 72 HOURS.

PURPOSE

ANTIMICROBIAL AGENT

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE

ETHYL ALCOHOL

INACTIVE INGREDIENT

WATER
ALOE VERA (ALOE BARBADENSIS) LEAF JUICE
ANHYDROUS CITRIC ACID
DIMETHICONE
ETHYLENE DIAMINE TETRAACETIC ACID TETRASODIUM SALT (EDTA-4Na)
HYDANTOINE
POLYSORBATE 20
TOCOPHERYL ACETATE (VITAMIN E)
GLYCERIN
FRAGRANCE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE

INDICATIONS AND USAGE

APPLY TO HANDS

ALLOW TO DRY WITHOUT WIPING

PACKAGE LABEL

INGREDIENTS AND APPEARANCE

MEDICALLY MINDED 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78502-6000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.25 g  in 100 g
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	93.885 g  in 100 g
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.05 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX)	0.5 g  in 100 g
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)	0.1 g  in 100 g
DIMETHICONE (UNII: 92RU3N3Y1O)	0.005 g  in 100 g
EDETATE SODIUM TETRAHYDRATE (UNII: L13NHD21X6)	0.008 g  in 100 g
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)	0.1 g  in 100 g
HYDANTOIN (UNII: I6208298TA)	0.002 g  in 100 g
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)	0.015 g  in 100 g
POLYSORBATE 20 (UNII: 7T1F30V5YH)	0.005 g  in 100 g
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)	0.08 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78502-6000-6	40 g in 1 BAG; Type 0: Not a Combination Product	06/28/2020
2	NDC: 78502-6000-7	30 g in 1 BAG; Type 0: Not a Combination Product	06/28/2020
3	NDC: 78502-6000-8	20 g in 1 BAG; Type 0: Not a Combination Product	06/28/2020
4	NDC: 78502-6000-9	10 g in 1 BAG; Type 0: Not a Combination Product	06/28/2020
5	NDC: 78502-6000-1	1 g in 1 BAG; Type 0: Not a Combination Product	06/28/2020
6	NDC: 78502-6000-2	5 g in 1 BAG; Type 0: Not a Combination Product	06/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/28/2020

Labeler - BELSKIN S. DE, R.L. DE C.V (816649743)

Registrant - BELSKIN S. DE, R.L. DE C.V (816649743)

Establishment
Name	Address	ID/FEI	Business Operations
BELSKIN S. DE, R.L. DE C.V		816649743	manufacture(78502-6000)