Label: LUCKY ANTIBACTERIAL- benzalkonium chloride liquid
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NDC Code(s):
20276-147-09,
20276-147-11,
20276-147-12,
20276-147-14, view more20276-147-15, 20276-147-16, 20276-147-40, 20276-147-64, 20276-147-75
- Packager: Delta Brands, Inc
- 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 January 14, 2021
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
- Inactive ingredients
- Package Label
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INGREDIENTS AND APPEARANCE
LUCKY ANTIBACTERIAL
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:20276-147 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 WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) COCO GLUCOSIDE (UNII: ICS790225B) GLYCERYL OLEATE (UNII: 4PC054V79P) GLYCERIN (UNII: PDC6A3C0OX) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) COCO MONOETHANOLAMIDE (UNII: C80684146D) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) SODIUM CHLORIDE (UNII: 451W47IQ8X) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:20276-147-12 400 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/10/2016 2 NDC:20276-147-75 221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/04/2020 3 NDC:20276-147-09 266 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/04/2020 4 NDC:20276-147-11 333 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/04/2020 5 NDC:20276-147-14 414 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/04/2020 6 NDC:20276-147-15 444 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/04/2020 7 NDC:20276-147-16 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/04/2020 8 NDC:20276-147-40 1180 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/04/2020 9 NDC:20276-147-64 1890 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/04/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/10/2016 Labeler - Delta Brands, Inc (102672008)