Family Wellness Ointment
NDC Package 69571-006-02
Package Information
Family Wellness (mineral oil, petrolatum, phenylephrine hcl) ointment is uses •helps relieve the local itching and discomfort associated with hemorrhoids.•Temporarily shrinks hemorrhoid tissue and relieves burning.•Temporarily provides a coating for relief of anorectal burning.•Temporarily protects the inflamed, irritated anorectal surface to help make bowel movements lesspainful. This formulation utilizes a ointment delivery system. Marketed by Front Pharmaceutical Plc, this product is identified by NDC 69571-006 and is authorized under FDA application M015.
Identification & Billing
- RxCUI: 1372298 - mineral oil 14 % / petrolatum 74.9 % / phenylephrine HCl 0.25 % Rectal Ointment
- RxCUI: 1372298 - mineral oil 0.14 MG/MG / petrolatum 0.749 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal Ointment
- RxCUI: 1372298 - mineral oil 14 % / petrolatum 74.9 % / phenylephrine hydrochloride 0.25 % Rectal Ointment
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 69571 - Front Pharmaceutical Plc
- 69571-006 - Family Wellness
- 69571-006-02 - 1 TUBE in 1 BOX / 57 g in 1 TUBE (69571-006-01)
- 69571-006 - Family Wellness
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 69571-006-02 identifies a specific commercial package of 1 tube in 1 box / 57 g in 1 tube (69571-006-01) of Family Wellness, a human over the counter drug labeled by Front Pharmaceutical Plc. This ointment is formulated for topical use and contains mineral oil; petrolatum; phenylephrine hydrochloride as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Front Pharmaceutical Plc on March 30, 2017. The current certification is valid through December 31, 2026.
How is this Front Pharmaceutical Plc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 69571000602. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.