OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Zinc Oxide 8.6% and Titanium Dioxide 6.5%
Sun Armor SPF 50
- Manufacturer
- Allure Labs, Inc
- Effective date
- 2017-11-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:53:11
Label at a glance#
ProductSun Armor SPF 50
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure10 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Purpose: Sunscreen
INDICATIONS & USAGE SECTION
Uses: To help protect the skin from harmful UVA and UVB rays. If used as directed with other sun protection measures, this product reduces the risk of skin cancer and early aging as well as helps prevent sunburn.
WARNINGS SECTION
Warnings: For external use only.
OTC - WHEN USING SECTION
When using this product: Keep out of eyes. If contacts occurs, rinse with water. Discontinue use if irritation or redness occurs.
OTC - STOP USE SECTION
Stop use and ask a doctor: If severe skin irritation develops.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Directions: Apply sunscreen in the AM to fingertips and gently massage into the skin. Reapply as needed.
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Water (Aqua), Cyclopenatasiloxane, C12-15 Alkyl Benzoate, Dimethicone, Cyclotetrasiloxane, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Alminum Hydroxide, Stearic Acid, Dimethicone/PEG-10/15 Crosspolymer, Glycerin, Sodium Chloride, Polyglyceryl-4 Isostearate, Cetyl PEG/PPG-10/1 Dimethicone, Hexyl Laurate, Cetearyl Olivate, Sorbitan Olivate, Cyclohexasiloxane, Tocopheryl Acetate, Hydrolyzed Vegetable Protein, Adenosine Triphosphate, Sodium Chondroitin Sulfate, PEG/PPG-18/18 Dimethicone, Dimethicone/Polyglycerin-3 Crosspolymer, Dimethicone / Vinyl Dimethicone Crosspolymer Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Ethylhexyl Palmitate, Silica Dimethyl Silylate, Butylene Glycol, Sodium Hyaluronate, Ectoin, Cyclotetrapeptide-24 Aminocyclohexane Carboxylate, Palmitoyl Oligopepetide, Palmitoyl Tetrapeptide-7, Vitis Vinifera (Grape) Fruit Cell Extract,Polygonum Aviculare Extract, Isomalt, Sodium Benzoate, Alcohol, Lecithin, Carbomer, Polysorbate 20, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol, PEG-8, Tocopherol, Ascorbic Acid, Ascorbyl Palmitate, Citric Acid.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Mnaufacture for Dermaquest Inc
Hayward, CA 94544
1272 GK, NL Made In USA
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| c5cd4727-ac49-4409-82b1-5bd8006c3ec7 | Product name | 1 | 20171122 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 62742-4096-2 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-82b7-a426-e053-dadaa90af4c2 | Drug facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62742-4096-1 | Sun Armor SPF 50 | 56.7 g in 1 TUBE | CREAM | 56.7 | 1 | |
| 62742-4096-2 | Sun Armor SPF 50 | 1 in 1 CARTON | CREAM | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 62742-4096 | SUN ARMOR SPF 50 (ZINC OXIDE AND TITANIUM DIOXIDE) CREAM [ALLURE LABS, INC] | 1 | Legacy NDC, 2 package rows | 20171202_6f108b71-b051-4163-8b17-c2481f60e3de.zip |
Products#
Every source-derived product name is available through these pages.
- Sun Armor SPF 50
- Zinc Oxide and Titanium Dioxide
- ZINC OXIDE
- TITANIUM DIOXIDE
- WATER
- CYCLOMETHICONE 5
- ALKYL (C12-15) BENZOATE
- DIMETHICONE
- ALUMINUM HYDROXIDE
- STEARIC ACID
- GLYCERIN
- SODIUM CHLORIDE
- POLYGLYCERYL-4 ISOSTEARATE
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2)
- HEXYL LAURATE
- CETEARYL OLIVATE
- SORBITAN OLIVATE
- CYCLOMETHICONE 6
- .ALPHA.-TOCOPHEROL ACETATE
- ADENOSINE TRIPHOSPHATE
- SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW)
- PEG/PPG-18/18 DIMETHICONE
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)
- ETHYLHEXYL PALMITATE
- SILICA DIMETHYL SILYLATE
- BUTYLENE GLYCOL
- HYALURONATE SODIUM
- ECTOINE
- PALMITOYL TETRAPEPTIDE-7
- WINE GRAPE
- POLYGONUM AVICULARE TOP
- ISOMALT
- SODIUM BENZOATE
- ALCOHOL
- EGG PHOSPHOLIPIDS
- CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)
- POLYSORBATE 20
- PHENOXYETHANOL
- CAPRYLYL GLYCOL
- ETHYLHEXYLGLYCERIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 62742-4096 | 62742-4096-1, 62742-4096-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| e1333fc1-1b2f-443f-9169-262ff17ab932 | 6f108b71-b051-4163-8b17-c2481f60e3de | 2017-11-29 | Warnings | e1333fc1-1b2f-443f-9169-262ff17ab932 6f108b71-b051-4163-8b17-c2481f60e3de |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.