NDC 69165-201 Antipain-s

NDC Product Code 69165-201

NDC 69165-201-51

Package Description: 1 TUBE in 1 BOX > 35 g in 1 TUBE (69165-201-21)

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

NDC Product Information

Antipain-s with NDC 69165-201 is a product labeled by George L. Rodriguez M.d., Pc. The generic name of Antipain-s is . The product's dosage form is and is administered via form.

Labeler Name: George L. Rodriguez M.d., Pc

Dosage Form: -

Product Type: 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.

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.

  • YELLOW WAX (UNII: 2ZA36H0S2V)
  • RICINUS COMMUNIS WHOLE (UNII: Q94QWM85RF)
  • PETROLATUM (UNII: 4T6H12BN9U)

Product Labeler Information

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

Labeler Name: George L. Rodriguez M.d., Pc
Labeler Code: 69165
Start Marketing Date: 08-12-2014 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 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.

Antipain-s 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

Otc - Active Ingredient

CONTENTS:EACH 1.0 GM CONTAINS:RADIX CLEMENTIS.....30 MGYELLOW WAX.....30 MGSEMEN MOMORDICAE.....15 MGSEMEN RICINI.....50 MGMYRRHA.....20 MGOLIBANUM.....20 MGMENTHOL.....50 MGMETHYL SALICYLATE.....10 MG

Otc - Purpose

PURPOSEPAIN RELIEF

Warnings

CAUTIONS:DO NOT USE THIS PRODUCT IF YOU HAVE A SENSITIVE SKIN.DO NOT APPLY TO THE WOUNDED OR DAMAGED SKIN.AVOID EYE CONTACT.DISCONTINUE USE IF SIGNS OF IRRITATION APPEAR. IF IRRITATION PERSISTS, CONSULT A DOCTOR. IF YOU ARE ALLERGIC TO ANY INGREDIENT IN THE PRODUCT, DO NOT USE.

Indications & Usage

RELIEVING SWELLING AND PAIN OF TRAUMA OR FRACTURE. RELIEVING THE PAIN OF LIMBS, SHOULDER AND BACK. RELIEVNG THE PAIN DUE TO DAMP AND CHILL.

Dosage & Administration

DIRECTIONS:FOR EXTERNAL USE ONLY.CLEAN THE UNCOMFORTABLE AREAS BEFORE APPLY. 3-4 TIMES PER DAY.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Inactive Ingredient

YELLOW WAX.....30 MGSEMEN RICINI.....50 MGPETROLATUM

* Please review the disclaimer below.