Active Ingredients
CAMPHOR
PETROLATUM
MENTHOL
Petrolatum
FDA Label NDC 73076-130
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Ishan Technology Co., Ltd for the product Petrolatum (NDC 73076-130). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, inactive ingredients, keep out of reach of children, consulting a coctor before using, stop use and ask a doctor, purpose, warnings, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredients
SOPHORA FLAVESCENS ROOT
VIOLAE HERBA
DICTAMNUS DASYCARPUS ROOT
ARNEBIAE RADIX
LONICERA LEAF AND STEM (TOP)
STELLERA CHAMAEJASME WHOLE
CNIDIUM MONNIERI FRUIT
ALOE
RHUS CHINENSIS MILL
LONICERA JAPONICA FLOWER
ZAOCYS DHUMNADES
STEARIC ACID
LIQUID PARAFFIN
vitamin E （ALPHA-TOCOPHEROL）
CHLORHEXIDINE ACETATE
BORNEOL
GLYCERIN
PURIFIED WATER
Keep Out Of Reach Of Children
if swallowed, call poison control or seek medical help
Consulting A Coctor Before Using
If pregnant or breast-feeding
Stop Use And Ask A Doctor
if condition worsens or does not improve within 7days
Purpose
analgesic, anesthetic, antipruritic
Warnings
For rectal use only
When Using This Product
do not get into eyes
Directions
Adults apply to the affected area up to 2-3 times daily clean affected area with mild soap and warm water, or sitz bath in
warm salt water, rinse thoroughly, and then gently dry (pat or blot with tissue or soft cloth before use)
Other Information
Store at room temperature.
* Please review the disclaimer below.
