Label: CHLORPHENIRAMINE MALEATE tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 67046-089-14, 67046-089-30 - Packager: Contract Pharmacy Services-PA
- This is a repackaged label.
- Source NDC Code(s): 0904-0012
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 January 10, 2011
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- Active ingredient
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have
- glaucoma
- trouble urinating due to an enlarged prostate gland
- a breathing problem such as emphysema or chronic bronchitis
- Directions
- Inactive ingredients
- QUESTIONS OR COMMENTS?
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INGREDIENTS AND APPEARANCE
CHLORPHENIRAMINE MALEATE
chlorpheniramine maleate tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67046-089(NDC:0904-0012) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE 4 mg Inactive Ingredients Ingredient Name Strength D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) LACTOSE (UNII: J2B2A4N98G) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color YELLOW Score 2 pieces Shape ROUND Size 8mm Flavor Imprint Code 44;194 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67046-089-14 14 in 1 BLISTER PACK 2 NDC:67046-089-30 30 in 1 BLISTER PACK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 01/10/2011 Labeler - Contract Pharmacy Services-PA (945429777)