- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children and pets
- Directions
- Other information
- Inactive Ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ZEP TRANQ MDW AB FOAM
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66949-387 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 mL Inactive Ingredients Ingredient Name Strength METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) HEXANEDIOL (UNII: ZIA319275I) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) WATER (UNII: 059QF0KO0R) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) GLYCERIN (UNII: PDC6A3C0OX) PHENOXYETHANOL (UNII: HIE492ZZ3T) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) LAUROYL/MYRISTOYL AMIDOPROPYL AMINE OXIDE (UNII: HY9O6ZW9CY) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) DI-PPG-2 MYRETH-10 ADIPATE (UNII: 4IN301M0KJ) TETRASODIUM IMINODISUCCINATE (UNII: GYS41J2635) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66949-387-04 6000 mL in 1 CASE; Type 0: Not a Combination Product 08/02/2017 2 NDC:66949-387-09 3300 mL in 1 CASE; Type 0: Not a Combination Product 08/02/2017 3 NDC:66949-387-24 15140 mL in 1 CASE; Type 0: Not a Combination Product 08/02/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/02/2017 Labeler - Zep Inc. (030471374) Establishment Name Address ID/FEI Business Operations Zep Inc. 112125310 manufacture(66949-387)