Label: ALLERGY RELIEF- chlorpheniramine maleate tablet
- NDC Code(s): 63868-333-24
- Packager: CHAIN DRUG MARKETING ASSOCIATION INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 1, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- difficulty in urination due to enlargement of the prostate gland
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Principal display panel
QC®
Quality
ChoiceNDC 63868-333-24
Allergy Relief
Chlorpheniramine maleate 4 mg
AntihistamineRelieves Sneezing, Runny Nose,
Itchy, Watery Eyes,
Itchy Throat4 Hour Relief
actual
size24 Tablets
TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF BLISTER UNIT IS TORN,
BROKEN OR SHOWS ANY SIGNS OF TAMPERING50844 ORG041919408
Distributed by C.D.M.A., Inc.©
43157 W 9 Mile Rd
Novi, MI 48375
www.qualitychoice.com
Questions: 800-935-2362Quality Choice 44-194
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
chlorpheniramine maleate tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-333 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 STARCH, CORN (UNII: O8232NY3SJ) D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6) ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) 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:63868-333-24 2 in 1 CARTON 07/08/2021 1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 07/08/2021 Labeler - CHAIN DRUG MARKETING ASSOCIATION INC (011920774) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(63868-333) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(63868-333) , pack(63868-333) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(63868-333) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(63868-333) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(63868-333)