Label: SLEEPINAL- diphenhydramine hydrochloride capsule
- NDC Code(s): 50486-616-16, 50486-616-32
- Packager: Blairex Laboratories, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 12, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each capsule)
- Purpose
- Use
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Warnings
Do not use
- in children under 12 years of age.
- with any other product containing diphenhydramine, even one used on skin.
Ask a doctor before use if you have
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- trouble urinating due to the enlargement of the prostate gland
- Directions
- Other information
- Inactive ingredients
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SLEEPINAL
diphenhydramine hydrochloride capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50486-616 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 50 mg Inactive Ingredients Ingredient Name Strength LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) TALC (UNII: 7SEV7J4R1U) MAGNESIUM STEARATE (UNII: 70097M6I30) GELATIN (UNII: 2G86QN327L) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 3 (UNII: PN2ZH5LOQY) Product Characteristics Color blue (transparent) Score no score Shape CAPSULE (CAPSULE) Size 19mm Flavor Imprint Code SLEEPINAL; Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50486-616-32 4 in 1 CARTON 10/01/1999 1 8 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:50486-616-16 2 in 1 CARTON 10/01/1999 2 8 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 M010 10/01/1999 12/31/2024 Labeler - Blairex Laboratories, Inc. (092575133)