Label: TRIAGE FIRST AID STATION- first aid kit kit
- NDC Code(s): 59898-902-01, 65517-0004-1, 65517-0019-1
- Packager: Dukal Corporation
- Category: MEDICAL DEVICE
Drug Label Information
Updated September 20, 2010
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- Official Label (Printer Friendly)
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PRINCIPAL DISPLAY PANEL
TRIAGE First Aid Station
3 PACK
Portable, convenient first aid pods to treat
Cuts and Scrapes, Bumps and BurnsCan be mounted or stand alone
(includes magnetic and adhesive strip)
Physicians Care® is a Registered Trademark of
ACME UNITED Corporation 60 Round Tree Hill Road, Fairfield CT 06824
Designed in the USA | Made in China
- CUTS AND SCRAPES Labeling
- BUMPS Labeling
- BURNS Labeling
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BZK Towelette Labeling
Reorder 855
NDC 65517-0004-1
Dukal
BZK TOWELETTE
Contains Benzalkonium Chloride
For External Use Only
Helps Prevent Infection
1 / Pouch
DUKAL CORPORATION
(631) 656-3800
Ronkonkoma, NY 11779 www.dukal.com
Made in China
Drug Facts
Active Ingredients..................... Benzalkonium Chloride 0.133% w/v
Purpose................................. First Aid Antiseptic
USE: Antiseptic Cleansing of face, hands and
body without soap and water. Airs dries in seconds
DO NOT USE: in the eyes or apply over large
areas of the body.
STOP USE: If irritation, redness or other symptoms
develop. Consult a doctor if the conditions persists
or gets worse.
CAUTION: Keep out of reach of children. If
swallowed get medical help or contact a Poison
Control Center right away.
DIRECTIONS: Tear open packet, unfold and use
as a washcloth.INACTIVE INGREDIENTS: Distilled Water
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First Aid Burn Cream Labeling
WaterJel
First Aid Burn Cream
Antiseptic Pain Relief with Aloe
Active Ingredients:
Benzalkonium Chloride 0.13%
Lidocaine HCL 0.5%
Water-Jel Technologies
Carlstadt, NJ 07072
Drug Facts
Purpose
First Aid Antiseptic, External analgesic
Uses
first aid to help prevent infection and for temporary
relief of pain an itching associated with minor cuts,
scrapes, burns
Warnings
For external use only
Do not use
in the eyes
in large quantities over raw or blistered areas or on
deep puncture wounds, animal bites, or serious burns
Keep out of reach of children
if ingested contact Poison Control Center right away
Directions
clean affected area apply a small amount not more
than 3 times daily may be covered with a sterile bandage
Other Information
Store at room temperature
- TRIAGE First Aid Station Label
- CUTS AND SCRAPES Label
- BUMPS Label
- BURNS Label
- BZK Towelette Label
- Burn Cream Label
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INGREDIENTS AND APPEARANCE
TRIAGE FIRST AID STATION
first aid kit kitProduct Information Product Type MEDICAL DEVICE Item Code (Source) NDC:65517-0019 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65517-0019-1 1 in 1 PACKAGE, COMBINATION Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 2 POUCH 2.8 mL Part 2 5 PACKET 4.5 g Part 1 of 2 BZK TOWELETTE
benzalkonium chloride swabProduct Information Item Code (Source) NDC:65517-0004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.00186 mL in 1.4 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 1.39814 mL in 1.4 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65517-0004-1 1.4 mL in 1 POUCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/01/2006 Part 2 of 2 FIRST AID BURN
lidocaine hydrochloride and benzalkonium chloride creamProduct Information Item Code (Source) NDC:59898-902 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g in 100 g Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM (UNII: 7FLD91C86K) LIGHT MINERAL OIL (UNII: N6K5787QVP) STEARIC ACID (UNII: 4ELV7Z65AP) POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A) CETYL ALCOHOL (UNII: 936JST6JCN) TROLAMINE (UNII: 9O3K93S3TK) GLYCERIN (UNII: PDC6A3C0OX) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) PROPYLPARABEN (UNII: Z8IX2SC1OH) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59898-902-01 0.9 g in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333 01/01/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333 05/01/2010 Labeler - Dukal Corporation (791014871)
