Label: BLUE CROSS LABORATORIES HAND RX- ethyl alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 22431-111-01, 22431-111-02 - Packager: Blue Cross Laboratories
- 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 March 8, 2011
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ACTIVE INGREDIENT
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
When using this product, do not use in or near the eyes. If contact occurs, rinse thoroughly with water.
Flammable. Keep away from fire of flame
For external use only
Stop use and ask a doctor if irritation or rash appears and lasts
Do not store above 110o F (43o C)
May discolor certain fabrics on surfaces - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BLUE CROSS LABORATORIES HAND RX
ethyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:22431-111 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) METHOXYISOPROPANOL (UNII: 74Z7JO8V3U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:22431-111-02 2 in 1 BOX 1 NDC:22431-111-01 59 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 05/01/2009 Labeler - Blue Cross Laboratories (008298879) Registrant - Ninghai Everstar Co. Ltd. (527072149) Establishment Name Address ID/FEI Business Operations Ninghai Everstar Co., Ltd. 527072149 manufacture