Label: HEMRID MEDICATED WIPES HEMORRHOIDAL WIPE WITH WITCH HAZEL AND ALOE- witch hazel cloth swab
-
Contains inactivated NDC Code(s)
NDC Code(s): 71430-100-10, 71430-100-48 - Packager: BELLIGADRIA SOLLUTIONS LLC
- 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 January 4, 2016
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
- When using this product
- Stop use and ask doctor if
- Keep out of reach of children
-
Directions
- open the lid on the top of the wipes pouch
- peel back wipes seal, remove completely and discard
- grab the top wipe at the edge of the center fold and pull out of pouch
- close lid after each use to retain moisture
- adults: 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 topical hemorrhoidal treatments and then discard
- children under 12 years of age consult a doctor
- Other information
- Iactive ingredients
- Questions or Comments
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
HEMRID MEDICATED WIPES HEMORRHOIDAL WIPE WITH WITCH HAZEL AND ALOE
witch hazel cloth swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71430-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL 0.5 g in 1 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) BENZALKONIUM (UNII: 7N6JUD5X6Y) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM CITRATE (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71430-100-48 48 in 1 BOX 05/01/2017 1 5.3 g in 1 POUCH; Type 0: Not a Combination Product 2 NDC:71430-100-10 10 in 1 BOX 05/01/2017 2 5.3 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part346 05/01/2017 Labeler - BELLIGADRIA SOLLUTIONS LLC (048891482) Registrant - BELLIGADRIA SOLLUTIONS LLC (048891482) Establishment Name Address ID/FEI Business Operations Hangzhou special nonwovens co.,ltd 420120734 manufacture(71430-100)