FDA.reportPublic FDA data

ProCure Zinc Oxide

Product NDC
55681-017
11-digit product format
556810017
Labeler code
55681
Product ID
55681-017_4ee11cb5-7447-6745-e063-6394a90a5fbf
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Twin Med LLC
Application
M016
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-06-16
Substance
ZINC OXIDE
Active strength
20 g/100g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
ProCure Zinc Oxide
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE20 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z
Rxcui198911

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55681-017-01ProCure Zinc Oxide28.3 g in 1 TUBEOINTMENT28.32
55681-017-02ProCure Zinc Oxide56.6 g in 1 TUBEOINTMENT56.62
55681-017-15ProCure Zinc Oxide425 g in 1 JAROINTMENT4252

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198911zinc oxide 20 % Topical OintmentPSN37a30ee5-fd33-b410-e063-6294a90aef722
198911zinc oxide 0.2 MG/MG Topical OintmentSCD37a30ee5-fd33-b410-e063-6294a90aef722
198911zinc oxide 20 % Topical OintmentSY37a30ee5-fd33-b410-e063-6294a90aef722
198911zinc oxide 200 MG per GM Topical OintmentSY37a30ee5-fd33-b410-e063-6294a90aef722
198911ZNO 0.2 MG/MG Topical OintmentSY37a30ee5-fd33-b410-e063-6294a90aef722

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
55681-017-015568100170128.3 g in 1 TUBE (55681-017-01) 28.3 g2025-06-16NoNoHistorical
55681-017-025568100170256.6 g in 1 TUBE (55681-017-02) 56.6 g2025-06-16NoNoHistorical
55681-017-1555681001715425 g in 1 JAR (55681-017-15) 425 g2025-06-16NoNoHistorical