UV Daily Hydration Tinted

Product NDC

72043-2816

11-digit product format

720432816

Labeler code

72043

Product ID

72043-2816_24789c51-5299-4660-9d21-38f665eb17a0

Type

HUMAN OTC DRUG

Nonproprietary name

octisalat and zinc oxide sunscreen

Dosage form

LOTION

Route

TOPICAL

Labeler

CP Skin Health Group, Inc

Application

M020

Marketing category

OTC MONOGRAPH DRUG

Marketing start

2026-05-18

Substance

OCTISALATE; ZINC OXIDE

Active strength

50; 110 g/1000g; g/1000g

Pharmacologic classes

Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]

NDC exclude flag

No

Listing certified through

2027-12-31

Current FDA listing

Yes