Active Ingredients
Homosalate (10.0%), Octinoxate (7.5%), Octisalate (5.0%), Octocrylene (10.0%), Oxybenzone (5.0%).
Waterblock Solar
FDA Label NDC 21839-091
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Gordon Laboratories, Inc for the product Waterblock Solar (NDC 21839-091). 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, other ingredients, otc - when using, otc - stop use, otc - do not use, other, principal display panel - 125 ml bottle carton, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Other Ingredients
Isododecane, Dicaprylyl Ether, Cyclopentasiloxane, Cocoglycerides, Butyloctyl Salicylate, Brassica Campestris/Aleurites Fordi Oil Copolymer, Diisopropyl Adipate, Melissa Officinalis Leaf Extract, Citrus Grandis (Grapefruit) Peel Oil, Retinyl Palmitate, Ascorbyl Palmitate, Limonene, Tocopheryl Acetate, Caprylyl Glycol.
Otc - When Using
For external use only, not to be swallowed. Avoid contact with eyes. If contact occurs, flush thoroughly with water.
Otc - Stop Use
If irritation develops, discontinue use.
Otc - Do Not Use
Do not use on infants under 6 months old.
Other
Dermalogica, Dist.
Los Angeles, CA 90009 USA
Principal Display Panel - 125 Ml Bottle Carton
waterblock
solar spray
spf 30
4.2 FL OZ / 125 ml e
dermalogica®
Principal Display Panel (125 ml Bottle Carton)
* Please review the disclaimer below.
