Label: SEACALL HYDROCORTISONE OINTMENT.- seacall hydrocortisone ointment ointment
- NDC Code(s): 76986-006-01
- Packager: Guangdong Quadrant Ecological Technology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 26, 2025
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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Active IngredientHYDROCORTISONE 0.1%
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PurposeRelief of dermatitis itching.
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UseUsed for pruritus, neurodermatitis, contact dermatitis, seborrheic dermatitis, chronic eczema.
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Warnings·For external use only. ·Not for infants. ·Use with caution in pregnant and lactating women. ·Prohibited for those who are allergic to this product. Allergic persons should be ...
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Do not useDo not use if the affected area has been broken, pus or obvious oozing or viral infections (such as herpes, blisters).
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When UsingWhen using this product, avoid contact with eyes, nose and mouth. If contact occurs, rinse thoroughly with water.
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Stop UseStop using and ask a doctor if any burning sensation, redness, or swelling at the site of application occurs or if symptoms are not relieved after 1 week of use.
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Ask DoctorIn case of accidental ingestion, get medical help or contact a poison control center immediately.
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Keep Out Of Reach Of ChildrenKeep out of reach of children. Children must be used under adults supervision.
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Directions1~2 times a day, take a small amount of application on the affected area and gently rub for a moment.
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Other informationOther Information - ·If you are using other drugs, please consult your physician or pharmacist before using this product. ·Athletes should use it with caution. ·Sealed, stored in a ...
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Inactive ingredientsMINERAL OIL,ZINC OXIDE,BEESWAX,COPERNICIA CERIFERA (CARNAUBA) WAX,POLYGLYCERYL-3 DIISOSTEARATE,TOCOPHERYL ACETATE,BISABOLOL,OCTYLDODECANOL,POLYGLYCERYL-10 DIOLEATE,BORNEOL,ECHIUM PLANTAGINEUM SEED ...
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PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCEProduct Information