Label: ONID WIPE- ethanol swab
- NDC Code(s): 71441-180-10
- Packager: ONID Technology 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 June 28, 2017
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Directions
- Keep Out of Reach of Children
- WARNINGS
- Inactive Ingredients
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
ONID WIPE
ethanol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71441-180 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) 24.9 mL in 100 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) 1 mL in 100 mL CHAMAECYPARIS OBTUSA WOOD OIL (UNII: P2OMP71Y62) .1 mL in 100 mL Product Characteristics Color white Score Shape RECTANGLE Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71441-180-10 .82 mL in 1 PACKET; Type 0: Not a Combination Product 06/28/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 06/28/2017 Labeler - ONID Technology Corp (658461764) Registrant - ONID Technology Corp (658461764) Establishment Name Address ID/FEI Business Operations Diamond Wipes International 161104729 manufacture(71441-180)
