87060-001 NDC - SEA JEWELS LEMON BALM FULL BODY SALVE (MELISSA OFFICINALIS LEAF, MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL, EUCALYPTUS OIL, COCONUT OIL, BEESWAX, ALPHA-TOCOPHEROL ACETATE DL-, FLAX SEED, ARGAN OIL, GRAPE SEED OIL, JOJOBA OIL, ARCTIUM LAPPA ROOT, OREGANO)

Drug Information

  • Product NDC: 87060-001
  • Proprietary Name: Sea Jewels Lemon Balm Full Body Salve
  • Non Proprietary Name: Melissa officinalis leaf, Melaleuca alternifolia (Tea Tree) leaf oil, Eucalyptus oil, Coconut oil, Beeswax, Alpha-tocopherol acetate DL-, Flax seed, Argan oil, Grape seed oil, Jojoba oil, Arctium lappa root, Oregano
  • Active Ingredient(s): 2.3 g/531.1g EUCALYPTUS OIL; 2.2 g/531.1g MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL; 7 g/531.1g MELISSA OFFICINALIS LEAF
  • Administration Route(s): TOPICAL
  • Dosage Form(s): SALVE

Labeler Information

Field Name Field Value
Labeler Name: SEAJewels LLC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:8/1/2025

Package Information

No. Package Code Package Description Billing Unit
187060-001-011 CANISTER in 1 CANISTER (87060-001-01) / 14.17 g in 1 CANISTER
287060-001-021 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (87060-001-02) / 113.4 g in 1 BOTTLE, PLASTIC

NDC Record

Field Name Field Value Definition
PRODUCT NDC87060-001The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMESea Jewels Lemon Balm Full Body SalveThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEMelissa officinalis leaf, Melaleuca alternifolia (Tea Tree) leaf oil, Eucalyptus oil, Coconut oil, Beeswax, Alpha-tocopherol acetate DL-, Flax seed, Argan oil, Grape seed oil, Jojoba oil, Arctium lappa root, OreganoThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESALVEThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE8/1/2025This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMESEAJewels LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEEUCALYPTUS OIL; MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL; MELISSA OFFICINALIS LEAFAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH2.3; 2.2; 7 
ACTIVE INGRED UNITg/531.1g; g/531.1g; g/531.1g 

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 12/19/2025

Previous Code
Next Code