10842-102 NDC - DOCTOR HOYS NATURAL PAIN RELIEF ()

Drug Information

Product NDC: 10842-102

Proprietary Name: Doctor Hoys Natural Pain Relief

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: DOCTOR HOY'S, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/10/2005

Package Information

No. Package Code Package Description Billing Unit
110842-102-01237 mL in 1 BOTTLE, DISPENSING (10842-102-01)
210842-102-021814 mL in 1 JUG (10842-102-02)
310842-102-03118 mL in 1 TUBE (10842-102-03)
410842-102-045 mL in 1 PACKET (10842-102-04)
510842-102-05946 mL in 1 JUG (10842-102-05)
610842-102-0889 mL in 1 BOTTLE, WITH APPLICATOR (10842-102-08)
710842-102-093785 mL in 1 JUG (10842-102-09)

NDC Record

Field Name Field Value Definition
PRODUCT NDC10842-102The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEDoctor Hoys Natural Pain ReliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/10/2005This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDOCTOR HOY'S, LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 5/3/2024