DSC Antibacterial Hand Soap LAVENDER

DSC Antibacterial Hand LAVENDER by

Drug Labeling and Warnings

DSC Antibacterial Hand LAVENDER by is a Otc medication manufactured, distributed, or labeled by Crystalline Heath & Beauty From The DEad Sea LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DSC ANTIBACTERIAL HAND LAVENDER- benzalkonium chloride soap 
Crystalline Heath & Beauty From The DEad Sea 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.

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DSC Antibacterial Hand Soap LAVENDER

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use

Helps eliminate bacteria on hands.

Warnings

For external use only.

When using this product

Avoid contact with eyes, ears and mouth. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor 

if irritaion or redness persists.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Use whenever washing your hands. Rinse with warm water.

Inactive ingredients:

Water/Aqua, Sodium Laureth Sulphate, Sodium Chloride, Cocamidopropyl Betaine, Glycerin, Maris Sal (Dead Sea Minerals), Fragrance (Parfum), Lavandula Angustifolia (Lavender) Oil, DMDM Hydantoin, Triethylene Glycol, Propylene Glycol, Benzyl Alcohol, Methylchloroisothiazolinone, Methylisothiazolinone, Magnesium Nitrate, Magnesium Chloride, Tetrasodium EDTA, Citric Acid.

Package Labeling:

DSC ANTIBACTERIAL HAND LAVENDER 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71095-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
LAVENDER OIL (UNII: ZBP1YXW0H8)
DMDM HYDANTOIN (UNII: BYR0546TOW)
TRIETHYLENE GLYCOL (UNII: 3P5SU53360)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BENZYL ALCOHOL (UNII: LKG8494WBH)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71095-005-00	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2020	12/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2020	12/31/2022

Labeler - Crystalline Heath & Beauty From The DEad Sea LTD (600582704)

Establishment
Name	Address	ID/FEI	Business Operations
Crystalline Heath & Beauty From The DEad Sea LTD		600582704	manufacture(71095-005)

Revised: 6/2022

Document Id: e069d7a5-45e6-e1ef-e053-2a95a90a04f6

34390-5

Set id: a79838d5-b7e8-0437-e053-2a95a90a56a9

Version: 2

Effective Time: 20220601

 

Crystalline