NDC 73703-125 Totaldry Medicated Soothing

NDC Product Information

Totaldry Medicated Soothing with NDC 73703-125 is product labeled by Secure Personal Care Products Llc. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:


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)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
  • CHOLECALCIFEROL (UNII: 1C6V77QF41)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • SAFFLOWER OIL (UNII: 65UEH262IS)
  • ALLANTOIN (UNII: 344S277G0Z)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • TROLAMINE (UNII: 9O3K93S3TK)

Product Labeler Information

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

Labeler Name: Secure Personal Care Products Llc
Labeler Code: 73703
Start Marketing Date: 06-01-2020 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: 12-31-2021 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.

Totaldry Medicated Soothing Product Label Images

Totaldry Medicated Soothing 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

Benzethonium Chloride 0.20%

Purpose

Antimicrobial

Uses

TotalDry™ Medicated & Soothing Cream, is a nongreasyantibacterial cream formulated for sensitve skin.

Warnings

For external use only. For external use only. If rashor irritation develops, discontinue use. Consult aphysician if irritation persists. Not for long-term use.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Directions

Apply a small amount of TotalDry™ Medicated &Soothing Cream to skin and rub in gently.

Ingredients

Water, Propanediol, Stearic Acid, Mineral Oil, CetylAlcohol, Dimethicone, Glyceryl Stearate, PEG-100Stearate, Sorbitan Oleate, Tocopheryl Acetate, RetinylPalmitate, Cholecalciferol, Aloe Barbadensis (Aloe Vera)Leaf Juice, Carthamus Tinctorius (Safflower) Seed Oil,Allantoin, Phenoxyethanol, Ethylhexylglycerin,Triethanolamine, Fragrance

* Please review the disclaimer below.