NDC 49035-751 Hygienic Cleansing Pad

NDC Product Code 49035-751

NDC CODE: 49035-751

Proprietary Name: Hygienic Cleansing Pad What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

  • 49035 - Wal-mart Stores Inc

NDC 49035-751-21

Package Description: 100 APPLICATOR in 1 JAR > 2.5 mL in 1 APPLICATOR

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Hygienic Cleansing Pad with NDC 49035-751 is a product labeled by Wal-mart Stores Inc. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 844379.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Wal-mart Stores Inc
Labeler Code: 49035
Start Marketing Date: 03-01-2007 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Hygienic Cleansing Pad Product Label Images

Hygienic Cleansing Pad Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Witch Hazel 50% v/v


Hemorrhoidal Astringent


For temporary relief of local discomfort, burning, and irritation associated with hemorrhoids


For external use only. Avoid contact with eyes.

Consult A Doctor

  • If condition worsens or does not improve within 7 daysin case of bleedingbefore exceeding the recommended dosage

Do Not

Put this product into rectum using fingers or any mechanical device or applicator

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.


  • When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly.Gently dry by patting or blotting with toilet tissue or soft cloth before each application of this product. Gently apply to the affected area by patting and then discard. Apply to the affected area up to 6 times daily or after each bowel movement. Children under 12 years of age: consult a doctor.

Other Information

Store at room temperature: 15°- 30° C (59° - 86° F)

Other Uses

For vaginal care - cleanse the area by gently wiping, patting or blotting with pad and discard. Repeat as needed.

Inactive Ingredients

Water, glycerin, alcohol 7% v/v, sodium citrate, propylene glycol, citric acid, diazolidinyl urea, methylparaben, propylparaben

Label Information

NDC 49035-751-21EQUATECompare to Tucks® active ingredient*Hygienic Cleansing Padspre-moistened hemorrhoidal/vaginal pads with witch hazelMEDICATED PADS100 PADSHygienic cleansing action for temporary relief of external rectal and vaginal itching and burningFor your protection, jar is sealed. Remove lid. If seal is broken or missing, do not use.*This product is not manufactured or distributed by Pfizer Consumer Healthcare, owner of the registered trademark TUCKS®.Manufactured by: Triad Pharmaceuticals, Inc. 700 West North Shore Drive, Hartland, WI 53029Serious side effects associated with use of this product can be reported to the phone number provided below. 1-800-288-1288

* Please review the disclaimer below.