NDC 68703-256 Sweat-less

Arg Nit, Castoreum, Humulus, Iodum, Kali Phos, Nat Mur

NDC Product Code 68703-256

NDC 68703-256-02

Package Description: 59 mL in 1 BOTTLE

NDC Product Information

Sweat-less with NDC 68703-256 is a a human over the counter drug product labeled by Silver Star Brands. The generic name of Sweat-less is arg nit, castoreum, humulus, iodum, kali phos, nat mur. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Silver Star Brands

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Sweat-less Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • SILVER NITRATE 6 [hp_C]/59mL
  • HOPS 30 [hp_C]/59mL
  • IODINE 30 [hp_C]/59mL
  • SODIUM CHLORIDE 6 [hp_X]/59mL

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.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Silver Star Brands
Labeler Code: 68703
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 06-07-2016 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: 12-31-2019 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: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Sweat-less 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

Hpus Active Ingredients:

Each dose contains equal parts of: Arg nit 6C, Castoreum 30C, Humulus 30C, Iodum 30C, Kali phos 30C, Nat mur 6X.


Homeopathic remedy for the relief of excessive sweating.*This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.


If symptoms persist or worsen, consult a healthcare professional. If pregnant or breastfeeding, ask a health professional before use. Keep this and all medication out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.


For all ages: Mix 0.50 mL in 1/4 cup water and sip slowly. Repeat 3-5 times daily as needed until symptoms subside. If preferred, drops may be taken directly into the mouth. Children under 12: Reduce serving to 0.25 mL, 3-5 times daily.

Other Safety Information

All Native Remedies health products are especially formulated by experts in the field of natural health and are manufactured according tot he highest pharmaceutical standards for maximum safety and effectiveness. For more information, visit us at
Contains no animal products, gluten, artificial flavors, preservatives, or colorants. Suitable for vegetarians.

Inactive Ingredients:

Purified water, USP grain alcohol (20% by volume)

Otc - Keep Out Of Reach Of Children

Keep this and all medication out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Otc - Pregnancy Or Breast Feeding

If pregnant or breastfeeding, ask a health professional before use.

Otc - Purpose

Reduces excessive perspiration

* Please review the disclaimer below.