PURE DASH Antiseptic Hand Soap ALMOND SCENTED

PURE DASH Antiseptic Hand ALMOND SCENTED by

Drug Labeling and Warnings

PURE DASH Antiseptic Hand ALMOND SCENTED by is a Otc medication manufactured, distributed, or labeled by Prime Lab, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURE DASH ANTISEPTIC HAND ALMOND SCENTED- benzalkonium chloride lotion 
Prime Lab, LLC

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PURE DASH Antiseptic Hand Soap ALMOND SCENTED

Durg Facts

Active ingredient

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.

Directions

Wet hands and forearms. Apply 5 milliliters (teaspoonful) or palmful to hands and forearms.scrub thoroughly for at least 30 seconds. Rinse and repeat.

Other information

• Protect from freezing
• Keep tightly closed in a dry, cool, and well-ventilated place

Inactive ingredients

Water, sodium lauryl sulfate, coco betaine, coconut diethanolamide, sodium chloride, fragrance, citric acid

Package Labeling:

PURE DASH ANTISEPTIC HAND ALMOND SCENTED 
benzalkonium chloride lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79937-011
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 0.001 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
COCO-BETAINE (UNII: 03DH2IZ3FY)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79937-011-00	3.8 L in 1 BOTTLE; Type 0: Not a Combination Product	02/15/2022	01/16/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	02/15/2022	01/16/2024

Labeler - Prime Lab, LLC (117553548)

Establishment
Name	Address	ID/FEI	Business Operations
Prime Lab, LLC		117553548	manufacture(79937-011)

Revised: 1/2024

Document Id: 0fb28392-af4d-9c25-e063-6294a90ace16

34390-5

Set id: 57306843-6b27-41b1-992d-ab19abc31f2c

Version: 3

Effective Time: 20240124