Non Tinted Ultra Zinc Face and Body

Product NDC
85698-205
11-digit product format
856980205
Labeler code
85698
Product ID
85698-205_45b3835d-49fb-c501-e063-6294a90ac628
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
LIV BODY AND BEAUTY LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-04-18
Substance
ZINC OXIDE
Active strength
200 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Non Tinted Ultra Zinc Face and Body
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE200 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85698-205-04Non Tinted Ultra Zinc Face and Body113 g in 1 BOTTLE, PUMPCREAM1132
85698-205-15Non Tinted Ultra Zinc Face and Body1.5 g in 1 PACKETCREAM1.52

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85698-205-0485698020504113 g in 1 BOTTLE, PUMP (85698-205-04) 113 g2023-04-18NoNoHistorical
85698-205-15856980205151.5 g in 1 PACKET (85698-205-15) 1.5 g2023-04-18YesNoHistorical