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Data / Drug companies / Elements Brands, Inc.

Elements Brands, Inc.: 7 products in the FDA NDC directory, labeler code 71221

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Elements Brands, Inc. (labeler code 71221) lists 7 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 7 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on June 1, 2018.

The request: Watch Elements Brands, Inc. (FDA labeler code 71221): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
71221
Products in commercial distribution
7
Packages
7
Finished drugs by generic name
1
Prescription products
0
Over the counter products
7
Flagged as original packager
7 of 7 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
February 21, 2017
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs7100%

Products by type

TypeProductsShare
Over the counter drugs7100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Titanium dioxide, zinc oxide7255

Dosage forms

Dosage formProductsShare
Cream7100%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
CoralSafe Broad Spectrum SPF3071221-333CreamOver the counter monograph drugsJune 1, 2018
Tropical Sands SPF-30 Broad Spectrum Sunscreen71221-796CreamOver the counter monograph drugsFebruary 24, 2017
Tropical Sands, SPF-50 Broad Spectrum Sunscreen71221-794CreamOver the counter monograph drugsFebruary 22, 2017
Tropical Sands SPF-30 Broad Spectrum Sunscreen (Coconut)71221-793CreamOver the counter monograph drugsFebruary 22, 2017
Tropical Sands SPF-30 Broad Spectrum Sunscreen71221-795CreamOver the counter monograph drugsFebruary 21, 2017
Coral Safe SPF-30 Broad Spectrum Sunscreen71221-792CreamOver the counter monograph drugsFebruary 21, 2017
Coral Safe SPF-30 Broad Spectrum Sunscreen71221-791CreamOver the counter monograph drugsFebruary 21, 2017

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.