NDC 70157-002

City Sunscreen serum Broad Spectrum SPF 30 Supergoop

Homosalate, Octisalate, Avobenzene, Octocrylene

City Sunscreen serum Broad Spectrum SPF 30 Supergoop is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Baxter Laboratories Pty. Ltd.. The primary component is Homosalate; Octisalate; Avobenzone; Octocrylene.

• Product ID: 70157-002_c5428a19-eb07-4b41-9e88-c3dcbf5aece8
• NDC: 70157-002
• Product Type: Human Otc Drug
• Proprietary Name: City Sunscreen serum Broad Spectrum SPF 30 Supergoop
• Generic Name: Homosalate, Octisalate, Avobenzene, Octocrylene
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2010-12-07
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part352
• Labeler Name: Baxter Laboratories Pty. Ltd.
• Substance Name: HOMOSALATE; OCTISALATE; AVOBENZONE; OCTOCRYLENE
• Active Ingredient Strength: 8 g/100mL; g/100mL; g/100mL; g/100mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 70157-002-01

50 mL in 1 BOTTLE, PUMP (70157-002-01)

• Marketing Start Date: 2010-12-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70157-002-06 [70157000206]

City Sunscreen serum Broad Spectrum SPF 30 Supergoop CREAM

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-07-19

NDC 70157-002-02 [70157000202]

City Sunscreen serum Broad Spectrum SPF 30 Supergoop CREAM

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-12-07

NDC 70157-002-03 [70157000203]

City Sunscreen serum Broad Spectrum SPF 30 Supergoop CREAM

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-12-07

NDC 70157-002-04 [70157000204]

City Sunscreen serum Broad Spectrum SPF 30 Supergoop CREAM

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-12-07

NDC 70157-002-01 [70157000201]

City Sunscreen serum Broad Spectrum SPF 30 Supergoop CREAM

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-12-07

NDC 70157-002-05 [70157000205]

City Sunscreen serum Broad Spectrum SPF 30 Supergoop CREAM

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-12-07

Drug Details

Active Ingredients

Ingredient	Strength
HOMOSALATE	8 g/100mL

OpenFDA Data

• SPL SET ID: a29e5a69-d17e-45ef-8dde-e99c6e4a2b22
• Manufacturer:
  • Baxter Laboratories Pty. Ltd.
• UNII:
  • G63QQF2NOX
  • 4X49Y0596W
  • 5A68WGF6WM
  • V06SV4M95S
• UPC Code:
  • 0894280001440
  • 0857250005428

NDC Crossover Matching brand name "City Sunscreen serum Broad Spectrum SPF 30 Supergoop" or generic name "Homosalate, Octisalate, Avobenzene, Octocrylene"

NDC	Brand Name	Generic Name
70157-002	City Sunscreen serum Broad Spectrum SPF 30	Homosalate, Octisalate, Avobenzene, Octocrylene
70157-003	City Sunscreen serum Broad Spectrum SPF 30	Homosalate, Octisalate, Avobenzene, Octocrylene
70157-004	City Sunscreen serum Broad Spectrum SPF 30	Homosalate, Octisalate, Avobenzene, Octocrylene
75936-111	City Sunscreen serum Broad Spectrum SPF 30	Homosalate, Octisalate, Avobenzene, Octocrylene
75936-221	City Sunscreen serum Broad Spectrum SPF 30	Homosalate, Octisalate, Avobenzene, Octocrylene
75936-222	City Sunscreen serum Broad Spectrum SPF 30	Homosalate, Octisalate, Avobenzene, Octocrylene