Label: SILADRYL ALLERGY MEDICINE- diphenhydramine hydrochloride liquid
- NDC Code(s): 54838-135-40, 54838-135-70, 54838-135-80
- Packager: Lannett Company, Inc.
- 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 April 23, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- Uses
- Warnings
- ASK DOCTOR
- ASK DOCTOR/PHARMACIST
- WHEN USING
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
-
Directions
- repeat dose every 4 to 6 hours
- do not take more than 6 doses in any 24-hour period
- Attention: use only enclosed dosing cup specifically designed for use with this product. Do not use any other dosing device.
adults and children 12 years and over
2 to 4 teaspoonfuls (TSP)
children 6 to under 12 years
1 to 2 teaspoonfuls (TSP)
children under 6 years
DO NOT USE Other information
Each 5 mL (1 TSP) contains: Sodium 14 mg. Store at room temperature 20°-25°C (68°-77°F). - repeat dose every 4 to 6 hours
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SILADRYL ALLERGY MEDICINE
diphenhydramine hydrochloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54838-135 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 12.5 mg in 5 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM CITRATE (UNII: 1Q73Q2JULR) SORBITOL (UNII: 506T60A25R) WATER (UNII: 059QF0KO0R) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C RED NO. 40 (UNII: WZB9127XOA) Product Characteristics Color Score Shape Size Flavor CHERRY (black cherry) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54838-135-40 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/1997 11/30/2024 2 NDC:54838-135-70 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/1997 11/30/2024 3 NDC:54838-135-80 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/1997 11/30/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 01/01/1997 11/30/2024 Labeler - Lannett Company, Inc. (002277481)