North Safety First Aid Kit 685533T13

Drug Labeling and Warnings

Drug Details [pdf]

NORTH SAFETY FIRST AID KIT 685533T13- benzalkonium chloride, water, ammonia 
Honeywell Safety Products USA, Inc

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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North Safety First Aid Kit 685533T13

BZK TOWELETTE

Active Ingredients

Benzalkonium Chloride, 0.133%

BZK TOWELETTE

Purpose

First Aid Antiseptic

BZK TOWELETTE

Use

Antiseptic Cleansing of face, hands, body without soap and water. Air dries in seconds.

BZK TOWELETTE

Do Not Use in the eyes or apply over large areas of the body.

BZK TOWELETTE

Stop Use if irritation, redness, or other symptoms develop. Consult a doctor if the conditon persists or gets worse.

BZK TOWELETTE

Caution Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

BZK TOWELETTE

Directions Tear open packet, unfold adn use as a washcloth.

BZK TOWELETTE

Inactive ingredients Sodium Bicarbonate, Water

EYE SALINE

Active ingredient:

Sterile water 99%

EYE SALINE

Purpose:

Eyewash

EYE SALINE

Uses

For flushing or irrigating the eye to remove loose foreign material, air pollutants, or chlorinated water.

EYE SALINE

Warnings

For external use only - Obtain immediate medical treatment for all open wounds in or near the eyes. To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard.

EYE SALINE

Do not use

  • if solution changes color or gets cloudy
  • with contact lenses
  • if twist-off cap is broken or missing
  • if the eye is lacerated or object is embedded

EYE SALINE

Stop use and consult a doctor if you have

  • changes in vision
  • continued redness, irritation or pain, or if the condition worsens or persists

EYE SALINE

Keep out of reach of children.

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

EYE SALINE

Directions

  • remove contacts before using
  • twist top to remove
  • flush the affected area as needed
  • control rate of flow by pressure on the bottle
  • if necessary, continue flushing with emergency eyewash or shower

EYE SALINE

Inactive ingredients

sodium chloride, sodium phosphate dibasic, sodium phosphate monobasic

EYE SALINE

Questions? Call 1-800-430-5490

Sperian Eye & Face Protection, Inc. (a Honeywell Company)

825 East Highway 151, Platteville, WI 53818 USA

AMMONIA INHALANT

ALCOHOL 35%. AMMONIA 15%

AMMONIA INHALANT

KEEP OUT OF REACH OF CHILDREN.

AMMONIA INHALANT

CRUSH ONCE, USE AND DISCARD

AMMONIA INHALANT

JAMES ALEXANDER CORPORATION

BZK TOWELETTE

DUKAL CORPORATION

NDC: 65517-0004-1

BZK TOWELETTE

Contains Benzalkonium Chloride

For External Use Only

DUKAL CORPORATION (631) 656-3800

Ronkonkoma, NY 11779 www.dukal.com

Made in China

Dukal BZK TWLT FrontDukal BZK TWLT Front

EYE SALINE

Honeywell

eye saline

EYEWASH

Sterile Isotonic Solution

1 fl.oz. (30 ml)

32-000457-0000 Buff Eyewash

AMMONIA INHALANT

0.3 ml AMMONIA INHALANT

A RESPIRATORY STIMULANT

FOR INHALATION ONLY

Ammonia Inh Front

Ammonia Inh Back

NORTH SAFETY FIRST AID KIT 685533T13 
benzalkonium chloride, water, ammonia kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 0498-8055
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 0498-8055-991 in 1 KIT10/01/201709/24/2019
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 16 POUCH 9 mL  in 1.4 
Part 20 BOTTLE, PLASTIC 1 mL  in 30 
Part 310 AMPULE 3 mL  in .3 
Part 1 of 3
BZK TOWELETTE 
benzalkonium chloride swab
Product Information
Item Code (Source)NDC: 65517-0004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.33 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 65517-0004-11.4 mL in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/22/2008
Part 2 of 3
SPERIAN EYESALINE EYEWASH 
water liquid
Product Information
Item Code (Source)NDC: 64809-101
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER99.8 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 64809-101-1230 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34909/22/2008
Part 3 of 3
AMMONIA INHALANTS 
ammonia inhalants inhalant
Product Information
Item Code (Source)NDC: 46414-3333
Route of AdministrationRESPIRATORY (INHALATION)
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA0.045 g  in 0.3 mL
Inactive Ingredients
Ingredient NameStrength
LAVENDER OIL (UNII: ZBP1YXW0H8)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
LEMON OIL (UNII: I9GRO824LL)  
NUTMEG OIL (UNII: Z1CLM48948)  
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 46414-3333-30.3 mL in 1 AMPULE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other09/22/2008
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other09/22/200809/24/2019
Labeler - Honeywell Safety Products USA, Inc (079287321)
Establishment
NameAddressID/FEIBusiness Operations
Honeywell Safety Products USA, Inc079287321pack(0498-8055)

Revised: 9/2019
Document Id: 9355bf18-d369-ecaa-e053-2995a90a162e
Set id: 593d673d-5e1c-2756-e053-2a91aa0a31e6
Version: 2
Effective Time: 20190924