NDC | 70140-001-16, 70140-001-30, 70140-001-36, 70140-001-40 |
Set ID | 5b34aa4c-725c-4756-e053-2a91aa0a27d9 |
Category | HUMAN OTC DRUG LABEL |
Packager | GULSAH URETIM PAZARLAMA - HUSEY IN KAYA |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333A |
- Active Ingredient
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use
- Keep out of reach of children
- Directions
- Inactive Ingredients
- Package Label
-
INGREDIENTS AND APPEARANCE
WET WIPES
benzalkonium chloride swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70140-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) BENZYL ALCOHOL (UNII: LKG8494WBH) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) EDETATE SODIUM (UNII: MP1J8420LU) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70140-001-30 30 in 1 PACKAGE; Type 0: Not a Combination Product 06/06/2016 2 NDC:70140-001-36 36 in 1 PACKAGE; Type 0: Not a Combination Product 06/06/2016 3 NDC:70140-001-40 40 in 1 PACKAGE; Type 0: Not a Combination Product 06/06/2016 4 NDC:70140-001-16 16 in 1 PACKAGE; Type 0: Not a Combination Product 06/06/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/06/2016 Labeler - GULSAH URETIM PAZARLAMA - HUSEY IN KAYA (356137617)