Label: PRE-MOISTENED TOWELETTE- chlorhexidine gluconate swab
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Contains inactivated NDC Code(s)
NDC Code(s): 80514-004-01 - Packager: JIANGSU HAIDA INTERNATIONAL TRADING CO., LTD.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated September 3, 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
- CAUTION: Keep out of reach of children
- Use
- Warnings
- Directions
- Inactive ingredients
- DRUG FACTS
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INGREDIENTS AND APPEARANCE
PRE-MOISTENED TOWELETTE
chlorhexidine gluconate swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80514-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE 0.2 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80514-004-01 1.2 g in 1 POUCH; Type 0: Not a Combination Product 09/04/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/04/2020 Labeler - JIANGSU HAIDA INTERNATIONAL TRADING CO., LTD. (546297290)