Label: SPRINSOL- chlorpheniramine maleate tablet
- NDC Code(s): 51467-101-01, 51467-101-02
- Packager: FORTUNE PHARMACAL COMPANY LIMITED
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 13, 2025
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR/PHARMACIST
-
WHEN USING
When using this product
do not exceed recommended dosage unless directed by a physician
may cause excitability especially in children
use caution when driving or operating machinery
avoid alcoholic beverages
may cause drowsiness; alcohol, sedatives, and tranquilizers may increase the drowsiness effect - PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
-
PRINCIPAL DISPLAY PANEL
Sprinsol
Safely Sealed
NDC 51467-101-02
Chlorpheniramine maleate - Antihistamine
temporarily relieves these symptoms due to hay fever (allergic rhinitis) or other upper respiratory allergies:
sneezing
runny nose
itching of the nose or throat
itchy, watery eyes36 Tablets
In Individually Sealed Strip
Respiratory Series

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INGREDIENTS AND APPEARANCE
SPRINSOL
chlorpheniramine maleate tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51467-101 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 SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STARCH, CORN (UNII: O8232NY3SJ) FD&C RED NO. 40 (UNII: WZB9127XOA) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) POVIDONE K30 (UNII: U725QWY32X) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) Product Characteristics Color red Score no score Shape ROUND Size 10mm Flavor Imprint Code FORTUNE Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51467-101-01 2 in 1 BOX 09/22/2017 1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:51467-101-02 3 in 1 BOX 09/22/2017 2 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 09/22/2017 Labeler - FORTUNE PHARMACAL COMPANY LIMITED (686280561) Registrant - FORTUNE PHARMACAL COMPANY LIMITED (686280561) Establishment Name Address ID/FEI Business Operations FORTUNE PHARMACAL COMPANY LIMITED 686280561 manufacture(51467-101)
