Sunsolve MD Firm and Replenish

Product NDC
84878-199
11-digit product format
848780199
Labeler code
84878
Product ID
84878-199_439594af-fc39-cec4-e063-6294a90a455f
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
LOTION
Route
TOPICAL
Labeler
Sunsolve MD Inc
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-11-06
Substance
ZINC OXIDE
Active strength
132 mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Sunsolve MD Firm and Replenish
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE132 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84878-199-01Sunsolve MD Firm and Replenish48 mL in 1 BOTTLE, PUMPLOTION484
84878-199-02Sunsolve MD Firm and Replenish1 in 1 CARTONLOTION14
84878-199-03Sunsolve MD Firm and Replenish13 mL in 1 BOTTLE, PUMPLOTION134
84878-199-04Sunsolve MD Firm and Replenish1 in 1 CARTONLOTION14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84878-199SUNSOLVE MD FIRM AND REPLENISH (ZINC OXIDE) LOTION [SUNSOLVE MD INC]2Current NDC, 4 package rows20250507_26f3417b-9ea4-e577-e063-6294a90ae53c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84878-199-018487801990148 mL in 1 BOTTLE, PUMP48 mlHistorical
84878-199-02848780199021 BOTTLE, PUMP in 1 CARTON (84878-199-02) / 48 mL in 1 BOTTLE, PUMP (84878-199-01) 2024-11-06NoNoHistorical
84878-199-038487801990313 mL in 1 BOTTLE, PUMP13 mlHistorical
84878-199-04848780199041 BOTTLE, PUMP in 1 CARTON (84878-199-04) / 13 mL in 1 BOTTLE, PUMP (84878-199-03) 2024-11-06NoNoHistorical