Label: PURA- witch hazel cloth
- NDC Code(s): 84217-050-48
- Packager: Mypura.com Limited
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of the 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 upto 6 times daily or after each bowel movement and before applying hemmorhoidal treatments and then discard.
- children under 12 years of age consult a doctor
- Flush or dispose of wipe in thrash
- For best results flush no more than one wipe at a time
- Inactive Ingredients
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Other Information
- store at room temperature 20 - 25 ºC (68 - 77ºF)
- 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 desired size and place in contact with tissue for a soothing and cooling effect. Leave in place for 15 minutesand repeat as needed.
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Principal Display Panel
Pura
48 medicated hemmorhoidal wipes
made from biodegradable plant fibers
Cooling and soothing Witch hazel
100% plastic-free flushable wipes
Pura's Pledge
We believe that you shouldn't have to choose between caring for your famile and caring for the environment. That's why we are on a mission to only create products that are good for people and planets.
48 WIPES - 7.7 X 6.3 IN
(195 X 160 MM)
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INGREDIENTS AND APPEARANCE
PURA
witch hazel clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84217-050 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 mg Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) COCOS NUCIFERA WHOLE (UNII: 245J88W96L) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) GLYCERIN (UNII: PDC6A3C0OX) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM BENZOATE (UNII: OJ245FE5EU) WATER (UNII: 059QF0KO0R) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84217-050-48 48 in 1 BOX 04/02/2024 1 1 in 1 PATCH; 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 04/02/2024 Labeler - Mypura.com Limited (225239472)