NDC | 59898-740-01, 59898-902-01, 65517-0004-1, 65517-0017-1 |
Set ID | 8066c3b9-ef8c-481d-8b16-8e7e8f2b947c |
Category | MEDICAL DEVICE |
Packager | Dukal Corporation |
Generic Name | |
Product Class | Amide Local Anesthetic, Aminoglycoside Antibacterial, Antiarrhythmic |
Product Number | |
Application Number | PART333 |
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HOW SUPPLIED
Weatherproof First Aid Kit
50 Person / Contains over 172 pieces
CLEANSE
Antiseptics
25 Antiseptic Towelettes
TREAT
Injury Treatment
1 Instant cold pack
1 Triangular BandageOintments
10 Burn cream packets
6 Triple Antibiotic OintmentPROTECT
Adhesive Bandages
100 Adhesive plastic bandages, 3/4” x 3”
16 Adhesive plastic bandages, 1" x 3"Non-Adhesive Bandages
1 Eye Pad 1 - 5/8" x 2 - 5/8"
4 Gauze pads 2" x 2"
6 Gauze pads 3" x 3'
1 Elastic bandageDressings
1 Absorbent pad 5" x 9"
Tape
1 First aid tape roll, 1/2” x 5 yds
Gloves
2 Medical grade gloves
Other
1 First aid handbook
1 Registration card
Implements
1 Scissors
1 Tweezers, plastic - GENERAL PRECAUTIONS
- REFERENCES
- PRINCIPAL DISPLAY PANEL
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Antiseptic Towelette Labeling
Reorder 51028
NDC 65517-0004-1
Physicians Care
Antiseptic Towelette
Contains Benzalkonium Chloride
For External Use Only
1 Prep Pad
Acme United Corporation, 60 Round Hill Road, Fairfield, CT 06824
Made in China
Drug Facts
Active Ingredients..................... Benzalkonium Chloride
Purpose................................. First Aid Antiseptic
Use First aid antiseptic to help prevent infection in minor cuts, scrapes and burns
Warnings
- For External Use Only
Do Not Use
- in the eyes or apply over large areas of the body. In case
of deep or puncture wounds, animal bites or serious burns, consult a doctor.
Stop Use and consult a doctor
If the condition persists or gets worse.
Do not use longer than 1 week unless directed by a doctor.
Keep out of reach of children. If swallowed get medical help or
contact a Poison Control Center right away.
Directions
Clean the affected area. Apply a small amount of this product
on the area 1 to 3 times daily. May be covered with a sterile
bandage - if bandaged, let dry first.
Other Information
Store at Room Temperature 15 - 30 C (59 - 86 F)
Inactive Ingredient purified water
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Triple Antibiotic Labeling
WaterJel
Triple Antibiotic
First Aid Ointment
To Help Prevent Infection
Each Gram contains
Bacitracin Zinc 400 units
Neomycin Sulphate 5 mg
(equivalent to 3.5 mg Neomycin base)
Polymyxin B Sulfate 5000 units
Water-Jel Technologies
Carlstadt, NJ 07072
Drug Facts
Uses to help prevent infection in
minor cuts, scrapes, burns
Warnings
For external use only
Do not use
in the eyes or apply over large areas of the body
If you are allergic to any of the ingredients
longer than 1 week unless directed by a doctor
Stop use and ask a doctor if
the condition persists or gets worse
a rash or other allergic reaction develops
Keep out of reach of children
if ingested contact Poison Control Center right away
Directions
clean affected area apply a small amount of product
(an amount equal to the surface area of the tip of a finger)
on the area 1 to 3 times daily may be covered with a sterile bandage
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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
- Weatherproof Kit Label
- Content Card Label
- BZK Towelette Label
- Triple Antibiotic Label
- Burn Cream Label
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INGREDIENTS AND APPEARANCE
WEATHERPROOF FIRST AID KIT
first aid kit kitProduct Information Product Type MEDICAL DEVICE Item Code (Source) NDC:65517-0017 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65517-0017-1 1 in 1 PACKAGE, COMBINATION Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 25 POUCH 35 mL Part 2 6 PACKET 5.4 g Part 3 10 PACKET 9.0 g Part 1 of 3 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 final part333 01/01/2006 Part 2 of 3 WATER-JEL 3-IN1 ANTIBIOTIC
bacitracin zinc, polymyxin b sulfate and neomycin sulfate ointmentProduct Information Item Code (Source) NDC:59898-740 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC 400 [iU] in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg in 1 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B SULFATE 5000 [iU] in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59898-740-01 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 Part 3 of 3 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)