Label: SHOPKO MAXIMUM STRENGTH MEDICATED WITH ALOE AND WITCH HAZEL- witch hazel cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 37012-121-50 - Packager: Shopko Stores Operating Co., LLC.
- Category: HUMAN OTC DRUG LABEL
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 July 16, 2013
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
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Directions
- adult: unfold wipe and cleanse the area by gently wiping, patting or blotting. If necessary, repeat until all matter is removed from the area.
- use up to 6 times daily or after each bowel movement and before applying hemorrhoidal treatments, and then discard
- Dispose of wipe in trash.
- For best results, only flush one or two wipes at a time.
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Other information
- store at room temperature 20-25°C (68-77°F)
- for vaginal care - cleanse the area by gently wiping, patting, or blotting. Repeat as needed.
- for use as moist compress - if necessary, first cleanse the area as previously described. Fold wipe to desire size and place in contact with tissue for a soothing and cooling effect. Leave in place for 15 minutes and repeat as needed.
- Inactive Ingredients
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
SHOPKO MAXIMUM STRENGTH MEDICATED WITH ALOE AND WITCH HAZEL
witch hazel clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37012-121 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL 50 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM BENZOATE (UNII: OJ245FE5EU) ALOE ARBORESCENS LEAF (UNII: 09TD8L5SQV) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37012-121-50 48 in 1 PACKAGE 1 2.9 g in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part346 07/16/2013 Labeler - Shopko Stores Operating Co., LLC. (023252638)