NDC 57934-0103 Antiperspirant Cedarwood

NDC Product Code 57934-0103

NDC 57934-0103-1

Package Description: 76 g in 1 TUBE

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

NDC Product Information

Antiperspirant Cedarwood with NDC 57934-0103 is a product labeled by Every Man Jack. The generic name of Antiperspirant Cedarwood is . The product's dosage form is and is administered via form.

Labeler Name: Every Man Jack

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.

  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • DICAPRYLYL ETHER (UNII: 77JZM5516Z)
  • STARCH, CORN (UNII: O8232NY3SJ)
  • HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
  • LEVANT COTTON SEED (UNII: 550E4N439V)
  • CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
  • MYRRH (UNII: JC71GJ1F3L)
  • USNEA BARBATA (UNII: D6DVA9TCAP)
  • CITRUS PARADISI SEED (UNII: 12F08874Y7)
  • CLARY SAGE OIL (UNII: 87L0D4U3M0)
  • ROSEMARY OIL (UNII: 8LGU7VM393)
  • GREEN TEA LEAF (UNII: W2ZU1RY8B0)

Product Labeler Information

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

Labeler Name: Every Man Jack
Labeler Code: 57934
Start Marketing Date: 06-01-2013 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.

Antiperspirant Cedarwood 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

Other

Drug Facts

Active Ingredient

Aluminum Chlorohydrate 23.0%,

Purpose

Anti-Perspirant

Use

  • Reduces underarm wetness

Warnings

For External Use Only

Otc - Do Not Use

Do not use on broken skin.

Otc - Ask Doctor

Ask a doctor before use if you have kidney disease.

Otc - Stop Use

Stop use if rash or irritation occurs.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply to underarms only

Inactive Ingredients

Isopropyl Myristate, Stearyl Alcohol, Dicaprylyl Ether, Corn Starch Modified, Hydrogenated Castor Oil, Gossypium Herbaceum (Cotton) Extract, Calendula Officinalis ExtractCertified Organic, Commiphora Myrrha (Myrrh) Gum, Usnea Barbata (Lichen) Extract, Citrus Grandis (Grapefruit) Seed Extract, Salvia Sclarea (Clary Sage) Oil, Rosmarinus Officinalis (Rosemary) Oil, Camellia Sinensis Leaf Extract, Fragrance.

* Please review the disclaimer below.