Label: TEACHER COLLECTION ANTI BACTERIAL COUNTRY APPLE- benzalkonium chloride lotion
TEACHER COLLECTION ANTI BACTERIAL SWEET APPLE- benzalkonium chloride lotion
TEACHER COLLECTION ANTI BACTERIAL DELICIOUS APPLE- benzalkonium chloride lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 75862-020-01, 75862-021-01, 75862-022-01 - Packager: GANZ U.S.A., LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 6, 2011
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Other information
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Inactive ingredients
Aqua (Water), Glycerin, Cetyl Alcohol, Glyceryl Stearate, Cetearyl Alcohol, Ceteareth-20, Dimethicone, Stearic Acid, Parfum (Fragrance), Althaea Officinalis Extract, Milk Lipid, Mangifera Indica (Mango) Seed Butter, Butyrospermum Parkii (Shea Butter), Ethylhexyl Palmitate, Petrolatum, Polyethylene, Tocopheryl Acetate, Phenoxyethanol, Caprylyl Glycol, Sorbic Acid, Carbomer, Sodium Hydroxide, Tetrasodium EDTA, Ultramarines. CONTAINS: Milk and Shea
- PRINCIPAL DISPLAY PANEL - 200 mL Sweet Apple Bottle Label
- PRINCIPAL DISPLAY PANEL - 200 mL Country Apple Bottle Label
- PRINCIPAL DISPLAY PANEL - 200 mL Delicious Apple Bottle Label
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INGREDIENTS AND APPEARANCE
TEACHER COLLECTION ANTI BACTERIAL COUNTRY APPLE
benzalkonium chloride lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75862-020 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 in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Cetyl Alcohol (UNII: 936JST6JCN) Glyceryl Monostearate (UNII: 230OU9XXE4) Cetostearyl Alcohol (UNII: 2DMT128M1S) Polyoxyl 20 Cetostearyl Ether (UNII: YRC528SWUY) Dimethicone (UNII: 92RU3N3Y1O) Stearic Acid (UNII: 4ELV7Z65AP) Althaea Officinalis Root (UNII: TRW2FUF47H) Cow Milk Fat (UNII: 463JZS0XJ3) Mangifera Indica Seed Butter (UNII: 4OXD9M35X2) Shea Butter (UNII: K49155WL9Y) Ethylhexyl Palmitate (UNII: 2865993309) Petrolatum (UNII: 4T6H12BN9U) High Density Polyethylene (UNII: UG00KM4WR7) Alpha-Tocopherol Acetate (UNII: 9E8X80D2L0) Phenoxyethanol (UNII: HIE492ZZ3T) Caprylyl Glycol (UNII: 00YIU5438U) Sorbic Acid (UNII: X045WJ989B) Carbomer Homopolymer Type C (UNII: 4Q93RCW27E) Sodium Hydroxide (UNII: 55X04QC32I) Edetate Sodium (UNII: MP1J8420LU) Ultramarine Blue (UNII: I39WR998BI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75862-020-01 200 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 11/30/2011 TEACHER COLLECTION ANTI BACTERIAL SWEET APPLE
benzalkonium chloride lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75862-021 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 in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Cetyl Alcohol (UNII: 936JST6JCN) Glyceryl Monostearate (UNII: 230OU9XXE4) Cetostearyl Alcohol (UNII: 2DMT128M1S) Polyoxyl 20 Cetostearyl Ether (UNII: YRC528SWUY) Dimethicone (UNII: 92RU3N3Y1O) Stearic Acid (UNII: 4ELV7Z65AP) Althaea Officinalis Root (UNII: TRW2FUF47H) Cow Milk Fat (UNII: 463JZS0XJ3) Mangifera Indica Seed Butter (UNII: 4OXD9M35X2) Shea Butter (UNII: K49155WL9Y) Ethylhexyl Palmitate (UNII: 2865993309) Petrolatum (UNII: 4T6H12BN9U) High Density Polyethylene (UNII: UG00KM4WR7) Alpha-Tocopherol Acetate (UNII: 9E8X80D2L0) Phenoxyethanol (UNII: HIE492ZZ3T) Caprylyl Glycol (UNII: 00YIU5438U) Sorbic Acid (UNII: X045WJ989B) Carbomer Homopolymer Type C (UNII: 4Q93RCW27E) Sodium Hydroxide (UNII: 55X04QC32I) Edetate Sodium (UNII: MP1J8420LU) Ultramarine Blue (UNII: I39WR998BI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75862-021-01 200 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 11/30/2011 TEACHER COLLECTION ANTI BACTERIAL DELICIOUS APPLE
benzalkonium chloride lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75862-022 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 in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Cetyl Alcohol (UNII: 936JST6JCN) Glyceryl Monostearate (UNII: 230OU9XXE4) Cetostearyl Alcohol (UNII: 2DMT128M1S) Polyoxyl 20 Cetostearyl Ether (UNII: YRC528SWUY) Dimethicone (UNII: 92RU3N3Y1O) Stearic Acid (UNII: 4ELV7Z65AP) Althaea Officinalis Root (UNII: TRW2FUF47H) Cow Milk Fat (UNII: 463JZS0XJ3) Mangifera Indica Seed Butter (UNII: 4OXD9M35X2) Shea Butter (UNII: K49155WL9Y) Ethylhexyl Palmitate (UNII: 2865993309) Petrolatum (UNII: 4T6H12BN9U) High Density Polyethylene (UNII: UG00KM4WR7) Alpha-Tocopherol Acetate (UNII: 9E8X80D2L0) Phenoxyethanol (UNII: HIE492ZZ3T) Caprylyl Glycol (UNII: 00YIU5438U) Sorbic Acid (UNII: X045WJ989B) Carbomer Homopolymer Type C (UNII: 4Q93RCW27E) Sodium Hydroxide (UNII: 55X04QC32I) Edetate Sodium (UNII: MP1J8420LU) Ultramarine Blue (UNII: I39WR998BI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75862-022-01 200 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 11/30/2011 Labeler - GANZ U.S.A., LLC (798785242)