Label: TUCKS MEDICATED COOLING PADS- witch hazel solution
- NDC Code(s): 10157-2103-1, 10157-2103-2, 10157-2103-3, 10157-2103-4
- Packager: Blistex Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 13, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only.
When using this product
- do not use more than directed unless told to do so by a doctor
- do not put directly in the rectum by using fingers or any mechanical device or applicator
-
Directions
Adults:
- when practical, clean the affected area with mild soap and warm water, and rinse thoroughly
- gently dry by patting or blotting with toilet tissue or a soft cloth before applying
- apply externally to the affected area up to 6 times daily or after each bowel movement
- after application, discard pad and wash hands
Children under 12 years of age: ask a doctor
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL - 100 Pad Jar Carton
-
INGREDIENTS AND APPEARANCE
TUCKS MEDICATED COOLING PADS
witch hazel solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10157-2103 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL 500 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM (UNII: 7FLD91C86K) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10157-2103-2 1 in 1 CARTON 08/30/2016 1 100 in 1 JAR 1 1 mL in 1 APPLICATOR; Type 0: Not a Combination Product 2 NDC:10157-2103-1 1 in 1 CARTON 08/30/2016 2 40 in 1 JAR 2 1 mL in 1 APPLICATOR; Type 0: Not a Combination Product 3 NDC:10157-2103-3 40 in 1 JAR 08/30/2016 3 1 mL in 1 APPLICATOR; Type 0: Not a Combination Product 4 NDC:10157-2103-4 2 in 1 CARTON 08/30/2016 4 100 in 1 JAR 4 1 mL in 1 APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M015 08/30/2016 Labeler - Blistex Inc (005126354) Establishment Name Address ID/FEI Business Operations Blistex Inc 005126354 manufacture(10157-2103)