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

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 - 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.

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.