Label: BD E-Z SCRUB 107- chlorhexidine gluconate solution
- NDC Code(s): 17271-107-03
- Packager: Becton Dickinson and Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated December 12, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
For external use only.
Do not use
- as a preoperative skin preparation of the face or head
- in eyes, ears and mouth
- if you have a sensitivity to chlorhexidine gluconate or its components.
When using this product
- avoid contact with meninges
- chlorhexidine gluconate has been reported to cause deafness when instilled in the middle ear through perforated ear drums
- chlorhexidine gluconate solution has been reported to cause serious and permanent eye injury when it has been permitted to enter and remain in the eye during surgical procedures
- if chlorhexidine gluconate solution should contact these areas, rinse out promptly and thoroughly with water.
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Directions
- wet hands and forearms to the elbows with warm water
- use nail cleaner and apply scrub solution from sponge side
- work up lather
- scrub nails, cuticles and interdigital spaces thoroughly for 3 minutes with brush side and hands and forearms with the sponge side
- rinse with warm water
- repeat scrub for 3 more minutes, use the sponge side only. Add water as necessary to produce the desired level of suds.
- rinse hands and arms thoroughly
- dry thoroughly
- Other information
- Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BD E-Z SCRUB 107
chlorhexidine gluconate solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17271-107 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE 40 g in 1000 mL Inactive Ingredients Ingredient Name Strength FD&C RED NO. 40 (UNII: WZB9127XOA) HYDROCHLORIC ACID (UNII: QTT17582CB) LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38) NONOXYNOL-12 (UNII: 6NR43D77O6) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) PEG-75 LANOLIN (UNII: 09179OX7TB) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17271-107-03 10 in 1 BOX 10/24/1989 1 30 in 1 CARTON 1 18 mL in 1 PACKAGE; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA072525 10/24/1989 Labeler - Becton Dickinson and Company (124987988) Establishment Name Address ID/FEI Business Operations Becton Dickinson and Company 124987988 manufacture(17271-107) , analysis(17271-107) , label(17271-107) , pack(17271-107)