Label: ANGEL OF MINE FOAMING HAND SANITIZER- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 33992-1450-8 - Packager: Greenbrier International, 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 15, 2021
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- Active ingredient
- Purpose
- Use
- 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
ANGEL OF MINE FOAMING HAND SANITIZER
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:33992-1450 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) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) WATER (UNII: 059QF0KO0R) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PEG-12 DIMETHICONE (UNII: ZEL54N6W95) TANGERINE PEEL (UNII: JU3D414057) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:33992-1450-8 236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/17/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/17/2020 Labeler - Greenbrier International, Inc (610322518) Establishment Name Address ID/FEI Business Operations Delta Kozmetik Sanayi Ve Ticaret-Selim Yesil 533151022 manufacture(33992-1450)