Search by Drug Name or NDC
NDC 30142-0188-16 Hemorrhoidal 14; 74.9; .25 g/100g; g/100g; g/100g Details
Hemorrhoidal 14; 74.9; .25 g/100g; g/100g; g/100g
Hemorrhoidal is a RECTAL OINTMENT in the HUMAN OTC DRUG category. It is labeled and distributed by Kroger Company. The primary component is MINERAL OIL; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE.
Product Information
NDC | 30142-0188 |
---|---|
Product ID | 30142-188_58e74823-36bf-4a35-8467-1c4c3f4e1515 |
Associated GPIs | |
GCN Sequence Number | 071294 |
GCN Sequence Number Description | phenyleph/mineral oil/petrolat OINT/APPL 0.25 %-14% RECTAL |
HIC3 | Q3D |
HIC3 Description | HEMORRHOIDAL PREPARATIONS |
GCN | 35039 |
HICL Sequence Number | 039599 |
HICL Sequence Number Description | PHENYLEPHRINE HCL/MINERAL OIL/PETROLATUM,WHITE |
Brand/Generic | Generic |
Proprietary Name | Hemorrhoidal |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | mineral oil, petrolatum, phenylephrine HCl |
Product Type | HUMAN OTC DRUG |
Dosage Form | OINTMENT |
Route | RECTAL |
Active Ingredient Strength | 14; 74.9; .25 |
Active Ingredient Units | g/100g; g/100g; g/100g |
Substance Name | MINERAL OIL; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE |
Labeler Name | Kroger Company |
Pharmaceutical Class | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part346 |
Listing Certified Through | 2024-12-31 |
Package
Package Images

NDC 30142-0188-16 (30142018816)
NDC Package Code | 30142-188-16 |
---|---|
Billing NDC | 30142018816 |
Package | 1 TUBE in 1 CARTON (30142-188-16) / 57 g in 1 TUBE |
Marketing Start Date | 2013-12-13 |
NDC Exclude Flag | N |
Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL 5c81d564-f786-46e1-af8b-f47521fbae60 Details
Uses
- •
- helps relieve the local itching and discomfort associated with hemorrhoids
- •
- temporarily shrinks hemorrhoidal tissue and relieves burning
- •
- temporarily provides a coating for relief of anorectal discomforts
- •
- temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful
Warnings
For external and/or intrarectal use only
Ask a doctor before use if you have
- •
- heart disease
- •
- high blood pressure
- •
- thyroid disease
- •
- diabetes
- •
- difficulty in urination due to enlargement of the prostate gland
Ask a doctor or pharmacist before use if you are
presently taking a prescription drug for high blood pressure or depression.
Keep out of reach of children.
Directions
- •
- adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe. Gently dry by patting or blotting with a tissue or a soft cloth before applying ointment.
- •
- when first opening the tube, puncture foil seal with top end of cap
- •
- apply to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movement
- •
- intrarectal use: remove cover from applicator, attach applicator to tube, lubricate applicator well and gently insert applicator into the rectum, thoroughly cleanse applicator after each use and replace cover
- •
- also apply ointment to external area
- •
- regular use provides continual therapy for relief of symptoms
- •
- children under 12 years of age: ask a doctor
Inactive ingredients
Package/Label Principal Display Panel
COMPARE TO the active ingredients of PREPARATION H® HEMORRHOIDAL OINTMENT
See back panel
OUR PHARMACIST RECOMMENDED
Hemorrhoidal Ointment
Prevents Further Irritation
Prompt, Soothing Relief from Painful Burning, Itching & Discomfort
Shrinks Swollen Hemorrhoidal Tissue
Protects Irritated Tissue
Relieves Internal & External Discomfort
NET WT 2 OZ (57g)
INGREDIENTS AND APPEARANCE
HEMORRHOIDAL
mineral oil, petrolatum, phenylephrine hcl ointment |
||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||
|
Labeler - Kroger Company (006999528) |
Revised: 12/2019
Document Id: 58e74823-36bf-4a35-8467-1c4c3f4e1515
Set id: 5c81d564-f786-46e1-af8b-f47521fbae60
Version: 5
Effective Time: 20191228