- Drug Facts
- Active ingredients
- Purpose
- Uses
- Warnings
- Keep out of reach of children.
- Directions
- Inactive ingredients
- Other information
- Questions? Call
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SPL UNCLASSIFIED SECTION
INSTRUCTIONS FOR USE: Apply to the affected area twice daily (or as needed) and massage gently.
Store in cool, dry place
AD1 ATOPIC DERMATITIS GEL
Atopic dermatitis is a skin alteration that consists of dry, flaky and irritated skin.
EBBE atopic dermatitis gel (AD1) hydrates and provides the emollience required to balance and restore the cutaneous barrier function.
The high molecular weight hyaluronic acid forms a protective film over the skin’s surface layers, thereby reducing the loss of transepidermal water and providing intense and prolonged hydration.
The formula contains ultra-purified seawater with more than 75 minerals and trace elements.
EBBE atopic dermatitis gel (AD1) reduces itching and flaking, whilst improving the skin’s hydration and elasticity.
The light texture is absorbed quickly.
Specially indicated for sensitive areas such as face, scalp, and groin.
Suitable for use on adults and children.
- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
EBBE
colloidal oatmeal gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71051-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y) OATMEAL 2 g in 100 mL Inactive Ingredients Ingredient Name Strength ACETYL HEXAPEPTIDE-49 (UNII: 4055X1S509) ALOE VERA LEAF (UNII: ZY81Z83H0X) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CARBENOXOLONE SODIUM (UNII: F1MP7242Z5) GLYCERIN (UNII: PDC6A3C0OX) HYALURONIC ACID (UNII: S270N0TRQY) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM HYDROXIDE (UNII: 55X04QC32I) EDETATE SODIUM (UNII: MP1J8420LU) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71051-101-02 1 in 1 BOX 11/05/2016 1 NDC:71051-101-01 100 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 11/05/2016 Labeler - BLUE SEA LABORATORIES SL. (466819309) Establishment Name Address ID/FEI Business Operations BLUE SEA LABORATORIES SL. 466819309 manufacture(71051-101)