NDC 48951-3188 Chamomilla 10 Special Order

NDC Product Code 48951-3188

NDC 48951-3188-5

Package Description: 60 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

Chamomilla 10 Special Order with NDC 48951-3188 is a product labeled by Uriel Pharmacy Inc.. The generic name of Chamomilla 10 Special Order is . The product's dosage form is and is administered via form.

Labeler Name: Uriel Pharmacy Inc.

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.

  • OLIVE OIL (UNII: 6UYK2W1W1E)
  • LANOLIN (UNII: 7EV65EAW6H)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • YELLOW WAX (UNII: 2ZA36H0S2V)
  • WATER (UNII: 059QF0KO0R)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • CITRUS PARADISI SEED (UNII: 12F08874Y7)

Product Labeler Information

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

Labeler Name: Uriel Pharmacy Inc.
Labeler Code: 48951
Start Marketing Date: 09-01-2009 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: 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.

Chamomilla 10 Special Order Product Label Images

Chamomilla 10 Special Order 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

Indications & Usage

Directions: FOR TOPICAL USE ONLY.

Dosage & Administration

Apply to skin as needed. Under age 2: Consult a doctor.

Otc - Active Ingredient

Active Ingredient: 100 gm contains: 10 gm Chamomilla e flor. 1X

Inactive Ingredient

Inactive Ingredients: Organic olive oil, Lanolin, White petrolatum, Beeswax, Distilled water, Potassium sorbate, Grapefruit seed extract

Otc - Purpose

Use: Temporary relief of cramps.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Warnings

Warnings: FOR EXTERNAL USE ONLY. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.

Otc - Questions

Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com

* Please review the disclaimer below.