KROGER MEDICATED WIPES HEMORRHOIDAL WIPE WITH WITCH HAZEL AND ALOE- witch hazel cloth swab 
The Kroger Co.

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.

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Kroger medicated wipes, NDC number 30142-791

Active ingredient

Witch hazel 50%

Purpose

Astringent

Uses

Warnings

For external use only

When using this product

Stop use and ask doctor if

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

Other information

Inactive ingredients

2-Bromo-2-Nitropropane-1,3-Diol, Aloe Barbadensis Leaf Juice, Citric Acid, Disodium Cocoamphodiacetate, Glycerin, Iodopropynyl Butylcarbamate, PEG-75 Lanolin, Propylene Glycol, Sodium Citrate, Water

Principal Display Panel - 48 ct packs

COMPARE TO active ingredient in PREPARATION H(R) MEDICATED WIPES*

Kroger Flusable Hemorrhoidal Medicated Wipes


Witch Hazel 50%

Gentle Everyday Cleansing to Reduce Irritation

PRE-MOISTENED

48 MEDICATED WIPES

5.0 in x 6.0 in (12.7 cm x 15.2 cm)

Flowrap

lidbox

KROGER MEDICATED WIPES  HEMORRHOIDAL WIPE WITH WITCH HAZEL AND ALOE
witch hazel cloth swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-791
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL0.5 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
BRONOPOL (UNII: 6PU1E16C9W)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PEG-75 LANOLIN (UNII: 09179OX7TB)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:30142-791-71252 g in 1 CONTAINER; Type 0: Not a Combination Product01/01/2023
2NDC:30142-791-9196 in 1 BOX01/01/2023
2504 g in 1 CONTAINER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34601/01/2023
Labeler - The Kroger Co. (006999528)
Registrant - Nice-Pak Products, Inc. (003778198)

Revised: 2/2023
Document Id: f4eb632b-0096-8e20-e053-2995a90a6e58
Set id: 48c1598d-6667-446f-ac90-10ab945d0617
Version: 7
Effective Time: 20230217
 
The Kroger Co.