Drug labels

Physical Daily Defense Broad Spectrum Sunscreen SPF 40

ZINC OXIDE · Private Label Skin Care · TOPICAL

HUMAN OTC DRUG
Open FDA's page for this record
Set ID
18444581-66a4-4eda-a8df-627fa3b4b98a
ID
18755e90-5ff9-4b42-b283-f54e2341852d
Effective time
20250226
Version
1
SPL product data elements

Physical Daily Defense Broad Spectrum Sunscreen SPF 40 Zinc Oxide ZINC OXIDE ZINC CATION WATER ISODODECANE PROPANEDIOL DIMETHICONE, UNSPECIFIED MEDIUM-CHAIN TRIGLYCERIDES POLYGLYCERYL-6 POLYRICINOLEATE POLYMETHYLSILSESQUIOXANE/TRIMETHYLSILOXYSILICATE BUTYLOCTYL SALICYLATE ALKYL (C12-15) BENZOATE COCOYL CAPRYLOCAPRATE POLYGLYCERYL-10 DIOLEATE DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) POLYHYDROXYSTEARIC ACID (2300 MW) PHENYLSILANETRIOL SOYBEAN LECITHIN DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) CITRUS BIOFLAVONOIDS GUAR GUM GLYCERIN SHEA BUTTER 1,2-HEXANEDIOL C18-36 ACID TRIGLYCERIDE TRIBEHENIN DISTEARDIMONIUM HECTORITE PROPYLENE CARBONATE AMINOMETHYLPROPANOL CAPRYLHYDROXAMIC ACID POLYSORBATE 20 PENTYLENE GLYCOL DECYL GLUCOSIDE XANTHAN GUM

SPL unclassified section

Drug Facts

brand MD Water Resistant (80 Minutes) Glycoproteins Bioflavonoids Lecithin MEDICAL GRADE SHIELD RECOMMENDED FOR • ALL SKIN TYPES GREEN LEAF PROGRAM NOT TESTED ON ANIMALS Distributed by: brandMD ® Canoga Park, CA 91304 (818) 534-3180 www.brandMD.com

Active ingredient
Active ingredient Zinc Oxide 17%
Purpose
Purpose Sunscreen
Indications and usage

Uses • Helps prevent sunburn • If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

Warnings For external use only Do not use • on damaged or broken skin When using this product • keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if • rash occurs Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Keep out of reach of children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Dosage and administration

Directions • Apply liberally on a clean dry face, avoiding delicate eye area 15 minutes before sun exposure • reapply: • after 80 minutes of swimming • or sweating • immediately after towel drying • at least every 2 hours • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: • limit time in the sun, especially from 10 a.m.– 2 p.m • wear long-sleeved shirts pants, hats, and sunglasses • children under 6 months of age: Ask a doctor

Storage and handling
Other information • protect the product in this container from excessive heat and direct sun
Inactive ingredient

Inactive ingredients Water/Aqua/Eau, Isododecane, Propanediol, Dimethicone, Caprylic/Capric Triglyceride, Polyglyceryl-6 Polyricinoleate, Polymethylsilsesquioxane/Trimethylsiloxysilicate, Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Coco-Caprylate/Caprate, Polyglyceryl-10 Dioleate, Dimethicone/Vinyl Dimethicone Crosspolymer, Polyhydroxystearic Acid, Polyphenylsilsesquioxane, Lecithin, Polysilicone-11, Fructooligosaccharide, Glycoproteins, Bioflavonoids, Guar (Cyamopsis Tetragonoloba) Gum, Glycerin, Shea (Butyrospermum Parkii) Butter, 1,2-Hexanediol, C18-36 Acid Triglyceride, Tribehenin, Disteardimonium Hectorite, Propylene Carbonate, Aminomethyl Propanol, Caprylhydroxamic Acid, Polysorbate 20, Pentylene Glycol, Decyl Glucoside, Xanthan Gum

Package label principal display panel
Packaging Sunscreen
Harmonized identifiers (openFDA)
Application number
M020
Brand name
Physical Daily Defense Broad Spectrum Sunscreen SPF 40
Generic name
ZINC OXIDE
Manufacturer name
Private Label Skin Care
Product NDC
72957-009
Product type
HUMAN OTC DRUG
Route
TOPICAL
Substance name
ZINC OXIDE
SPL ID
18755e90-5ff9-4b42-b283-f54e2341852d
SPL set ID
18444581-66a4-4eda-a8df-627fa3b4b98a
Package NDC
72957-009-01
Original packager product NDC
39765-050
UNII
SOI2LOH54Z
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.