NDC 62296-7031

ULTA TANNING SPF 4

Octinoxate, Padimate O

ULTA TANNING SPF 4 is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Ulta. The primary component is Octinoxate; Padimate O.

• Product ID: 62296-7031_b909a65b-a935-4cbe-9e06-e0c2882ed020
• NDC: 62296-7031
• Product Type: Human Otc Drug
• Proprietary Name: ULTA TANNING SPF 4
• Generic Name: Octinoxate, Padimate O
• Dosage Form: Lotion
• Route of Administration: TOPICAL
• Marketing Start Date: 2015-08-03
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part352
• Labeler Name: Ulta
• Substance Name: OCTINOXATE; PADIMATE O
• Active Ingredient Strength: 2 g/100g; g/100g
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 62296-7031-6

236 g in 1 BOTTLE (62296-7031-6)

• Marketing Start Date: 2015-08-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 62296-7031-6 [62296703106]

ULTA TANNING SPF 4 LOTION

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-08-03
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
OCTINOXATE	2 g/100g

OpenFDA Data

• SPL SET ID: 4e600038-f9f0-49df-8f74-ca8a3e3d7d7e
• Manufacturer:
  • Ulta
• UNII:
  • Z11006CMUZ
  • 4Y5P7MUD51

NDC Crossover Matching brand name "ULTA TANNING SPF 4" or generic name "Octinoxate, Padimate O"

NDC	Brand Name	Generic Name
62296-7031	ULTA TANNING SPF 4	Octinoxate, Padimate O
63354-031	BANANA BOAT	octinoxate, padimate o
30142-929	KROGER SPF 4 TANNING OIL	OCTINOXATE, PADIMATE O
41250-039	MEIJER SPF 4 TANNING OIL	OCTINOXATE, PADIMATE O