![BZK ANTISEPTIC TOWELETTE (BENZALKONIUM CHLORIDE) SWAB [GUANGDONG COMFORT MEDICAL PRODUCTS CO., LTD.]](https://medic.hrt.org//dailymed/images/548cc932-c4ea-3360-e054-00144ff88e88/other.jpg)
| NDC | 71584-0103-1 |
| Set ID | 548cc932-c4ea-3360-e054-00144ff88e88 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | Guangdong Comfort Medical Products Co., Ltd. |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number | PART333A |
- INACTIVE INGREDIENTS
- DIRECTIONS
-
WARNINGS
WARNINGS
For external use only.
DO NOT USE, in the eyes. If this happens, rinse thoroughly with water.
STOP USE and ASK A DOCTOR: If irritation or redness develop and persists for more than 72 hours.
CAUTION: Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away. - USES
- CAUTION: Keep out of reach of children
- PURPOSE
- ACTIVE INGREDIENT
-
Drug Facts
ACTIVE INGREDIENT
Benzalkonium chloride 0.13% PURPOSE
First Aid Antiseptic USES
Antiseptic cleansing of face, hands and body to decrease bacteria on skin without soap and water. WARNINGS
For external use only.
DO NOT USE, in the eyes. If this happens, rinse thoroughly with water.
STOP USE and ASK A DOCTOR: If irritation or redness develop and persists for more than 72 hours.
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. Allow hands to dry without wiping. OTHER INFORMATION
Store at room temperature. INACTIVE INGREDIENTS
Water.
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INGREDIENTS AND APPEARANCE
BZK ANTISEPTIC TOWELETTE
benzalkonium chloride swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71584-0103 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:71584-0103-1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product 07/17/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/17/2017 Labeler - Guangdong Comfort Medical Products Co., Ltd. (544507534) Registrant - Guangdong Comfort Medical Products Co., Ltd. (544507534)