Label: WIPES PLUS- alcohol swab
-
Contains inactivated NDC Code(s)
NDC Code(s): 67151-606-01, 67151-606-02, 67151-606-03 - Packager: Progressive Products, LLC
- Category: HUMAN OTC DRUG LABEL
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 14, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive Ingredients
- Questions or Comments
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
WIPES PLUS
alcohol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67151-606 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67151-606-01 80 in 1 PACKAGE 09/01/2020 1 1 mL in 1 PACKAGE; Type 0: Not a Combination Product 2 NDC:67151-606-02 240 in 1 PACKAGE 09/01/2020 2 1 mL in 1 PACKAGE; Type 0: Not a Combination Product 3 NDC:67151-606-03 1500 in 1 PACKAGE 09/01/2020 3 1 mL in 1 PACKAGE; 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 part333E 09/01/2020 Labeler - Progressive Products, LLC (127111792) Registrant - Progressive Products, LLC (127111792)