Label: ANTIBACTERIAL HAND UNICORN SPRINKLES- benzalkonium chloride soap
- NDC Code(s): 41250-755-01
- Packager: Meijer Distribution 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 20, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
- Warnings
- Directions
- Inactive Ingredients
- Questions?
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
ANTIBACTERIAL HAND UNICORN SPRINKLES
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-755 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1 mg in 1 mL Inactive Ingredients Ingredient Name Strength OLIVE OIL (UNII: 6UYK2W1W1E) PEG-7 STEARATE (UNII: VCX261B12R) WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-755-01 295 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 10/30/2020 Labeler - Meijer Distribution Inc. (006959555)