Label: UP AND UP MEDICATED WIPES MANIXIM STRENGTH- gentle hemorrhoidal care swab
- NDC Code(s): 11673-404-48, 11673-404-96
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 7, 2024
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 a doctor if
- Keep out of reach of children.
-
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 topical hemorrhoidal treatments, and then discard
- children under 12 years of age: consult a doctor
- Other information
- Inactive ingredients
-
Principal display panel- 48 count
Compare to active ingredient in Preparation H Medicated Wipes
Maximum strength medicated wipes
gentle hemorrhoidal care
with witch hazel and aloe to cool, soother and comfort
48 medicated wipes
6 in x 5in (15.2cm x 12.7 cm)
Other Uses:
• for vaginal care - cleanse the area by gently wiping, patting or blotting. Repeat as needed.
• for use as a 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 minutes and repeat as needed.Flowrap of 48 counts:
lid
Box of 96 counts containing 2 flowraps:
-
INGREDIENTS AND APPEARANCE
UP AND UP MEDICATED WIPES MANIXIM STRENGTH
gentle hemorrhoidal care swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-404 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 ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM CITRATE (UNII: 1Q73Q2JULR) BRONOPOL (UNII: 6PU1E16C9W) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) PEG-75 LANOLIN (UNII: 09179OX7TB) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-404-96 2 in 1 CARTON 04/03/2019 1 48 in 1 CELLO PACK 1 5.375 g in 1 APPLICATOR; Type 0: Not a Combination Product 2 NDC:11673-404-48 48 in 1 CELLO PACK 01/01/2015 2 5.375 g 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 01/01/2015 Labeler - Target Corporation (006961700) Registrant - Nice-Pak Products, Inc. (003778198) Establishment Name Address ID/FEI Business Operations Nice-Pak Products, Inc. 067900167 manufacture(11673-404)