- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
- Questions
- BZK Active ingredient
- BZK Purpose
- BZK Uses
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BZK
Warnings
For external use only
Do not use
- in the eyes or over large areas of the body
- on mucous membranes
- on irritated skin
- in case of deep puncture wounds, animal bites or serious burns, consult a doctor
- longer than 1 week unless directed by a doctor
- BZK Directions
- BZK Other information
- BZK Inactive ingredient
- BZK Questions
- 4268 SF00000669 Kit Contents
- PAWS Principal Display Panel
- BZK Principal Display Panel
- 4268 Kit Label SF00000669
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INGREDIENTS AND APPEARANCE
4268 FIRST AID KIT
4268 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4268 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4268-01 1 in 1 KIT 10/13/2018 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 3 PACKET 0.0057 L Part 2 1 PACKET 1.4 mL Part 1 of 2 ANTIMICROBIAL
alcohol liquidProduct Information Item Code (Source) NDC:61010-3111 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 665 mL in 1 L Inactive Ingredients Ingredient Name Strength ALOE (UNII: V5VD430YW9) WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 10 in 1 BOX 1 0.0019 L in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/21/2017 Part 2 of 2 ANTISEPTIC TOWELETTE
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 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 WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0501-00 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/13/2018 Labeler - Honeywell Safety Products USA, Inc. (079287321) Registrant - Honeywell Safety Products US, Inc. (079287321) Establishment Name Address ID/FEI Business Operations Honeywell Safety products USA, Inc. 079287321 pack(0498-4268) Establishment Name Address ID/FEI Business Operations Changzhou Maokang Medical 421317073 manufacture(0498-0501) Establishment Name Address ID/FEI Business Operations Safetec of America 874965262 manufacture(61010-3111)