NDC | 57702-464-00, 57702-464-03, 57702-464-13 |
Set ID | dbaf3296-49d4-472a-909b-df46556095af |
Category | HUMAN OTC DRUG LABEL |
Packager | Bocchi Laboratories Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333E |
- Active Ingredients
- Purpose
- Uses
- Warnings
- Keep out of reach of children.
- Directions
- Other Information
- Inactive ingredients
- Active Ingredients
- Purpose
- Uses
-
Warnings
- For external use only.
- Flammable, keepaway from flame.
- Avoid contact with eyes. In case of eye contact, rinse eyes thoroughly with water.
- Discontinue use if irritation and redness develops. Consult a doctor if condition persists for more than 72 hours.
- If swallowed, immediately call Poison Control Center or doctor.
- Directions
- Other Information
- Inactive Ingredients
- Package/Label Principal Display Panel
- Package/Label Principal Display Panel
- Package/Label Principal Display Panel
-
INGREDIENTS AND APPEARANCE
ZYLAST ANTISEPTIC
ethyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57702-464 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.76 mL in 1 mL Inactive Ingredients Ingredient Name Strength FARNESOL (UNII: EB41QIU6JL) WATER (UNII: 059QF0KO0R) POLIHEXANIDE (UNII: 322U039GMF) PANTHENOL (UNII: WV9CM0O67Z) BENZETHONIUM CHLORIDE (UNII: PH41D05744) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57702-464-00 59.1 mL in 1 BOTTLE 2 NDC:57702-464-03 236.6 mL in 1 BOTTLE 3 NDC:57702-464-13 1000 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 06/01/2011 Labeler - Bocchi Laboratories Inc. (078376306)