doTERRA sun

Product NDC
71630-966
11-digit product format
716300966
Labeler code
71630
Product ID
71630-966_2ccc9cfb-f2f7-4663-e063-6294a90aa0e5
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
LOTION
Route
TOPICAL
Labeler
doTERRA International, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-06-01
Substance
ZINC OXIDE
Active strength
16.3 g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
doTERRA sun
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE16.3 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71630-966-50doTERRA sun142 g in 1 TUBELOTION1422

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71630-966DOTERRA SUN (ZINC OXIDE) LOTION [DOTERRA INTERNATIONAL, LLC]2Current NDC, Legacy NDC, 1 package rows20250207_dd2fa6a2-2ba8-4333-e053-2a95a90a9790.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71630-966-5071630096650142 g in 1 TUBE (71630-966-50) 142 g2022-06-010000-00-00NoNoCurrent