58443-0302 : Aloe Up Topical Spray


NDC: 58443-0302
Labeler: Prime Enterprises Inc.
Product Type: Human OTC Drug
Drug Name: Aloe Up Broad Spectrum Spf 50 Sunscreen
Dosage Form: Topical Spray
Application #: part352
Rev. Date: 


NDC Package Codes:

  • 58443-0302-4: 177 ML IN 1 BOTTLE (58443‑0302‑4)

Active Ingredients:

  • Homosalate
  • Octocrylene
  • Avobenzone
  • Octisalate
  • Octinoxate

Dosage Strength:

  • 49.7 mg/mL
  • 99.4 mg/mL
  • 29.82 mg/mL
  • 49.7 mg/mL
  • 59.64 mg/mL

Related Products:

Based on records with the same trade name.
  • 58443-0300 Aloe Up Topical Spray by Prime Enterprises Inc.
  • 58443-0559 Aloe Up Topical Lotion by Prime Enterprises Inc.
  • 58443-0560 Aloe Up Topical Lotion by Prime Enterprises Inc.
  • 13630-0181 Aloe Up Topical Spray by Prime Packaging Inc.
  • 13630-0183 Aloe Up Topical Spray by Prime Packaging Inc.
  • 13630-0207 Aloe Up Topical Spray by Prime Packaging Inc.
  • 13630-0208 Aloe Up Topical Spray by Prime Packaging Inc.
  • 13630-0257 Aloe Up Topical Spray by Prime Packaging Inc.

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 58443-0302 QR Code

< Prev: 58443-0301Next: 58443-0303 >

Related Discussions:

homosalate oxybenzone
affects on gender, gender bender?...




Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.