Label: BRIZZEL- alcohol cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 80303-001-01 - Packager: MAGS CHEM CORP
- 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 October 13, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Warnings
- Keep out of reach of children.
- Uses
- Directions
- Inactive Ingredients
- Product Label
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INGREDIENTS AND APPEARANCE
BRIZZEL
alcohol clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80303-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) BENZETHONIUM CHLORIDE (UNII: PH41D05744) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80303-001-01 100 in 1 CANISTER 10/10/2020 1 2.82 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/10/2020 Labeler - MAGS CHEM CORP (131425059)
