Ebbe
FDA Label NDC 71051-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Blue Sea Laboratories Sl. for the product Ebbe (NDC 71051-101). 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 drug facts, active ingredients, purpose, uses, warnings, keep out of reach of children., directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Colloidal Oatmeal 2%
Purpose
Skin protectant
Uses
Temporarily protects and helps relieve minor skin irritation and itching due to: ■ Eczema ■ Rashes
Warnings
For external use only.
When using this product
■ do not get into the eyes.
Stop use and ask a doctor if
■ condition worsens.
■ symptoms last more than 7 days or clear up and occur again within a few days.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a poison control center immediately.
Directions
Apply as needed.
Inactive Ingredients
acetyl hexapeptide-49, aloe barbadensis (aloe vera) leaf juice, caprylhydroxamic acid, caprylyl glycol, disodium succinoyl glycyrrhetinate, glycerin, hyaluronic acid, seawater, sodium hydroxide, tetrasodium EDTA, xanthan gum
Other Information
For use on mild to moderate eczema or as directed by a physician. Store at room temperature. You may report serious side effects to the phone number provided under Questions? below.
Questions? Call
844-EBBE-866
* Please review the disclaimer below.
