Label: ALCOHOL swab
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Contains inactivated NDC Code(s)
NDC Code(s): 70082-001-01, 70082-001-02, 70082-001-03 - Packager: DealmedMedical Supplies LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 November 18, 2022
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Uses: alcohol
- Warnings:
- Do not use:
- Stop use and ask a doctor:
- Keep Out Of Reach Of Children
- Directions:
- Inactive Ingredient
- Indications and Usage:
- Principal display panel
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INGREDIENTS AND APPEARANCE
ALCOHOL
alcohol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70082-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70082-001-01 200 in 1 BOX 06/04/2018 1 3 mL in 1 POUCH; Type 0: Not a Combination Product 2 NDC:70082-001-02 100 in 1 BOX 06/04/2018 2 3 mL in 1 POUCH; Type 0: Not a Combination Product 3 NDC:70082-001-03 300 in 1 BOX 06/05/2018 3 3 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part344 09/15/2015 Labeler - DealmedMedical Supplies LLC (068586441)
