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Dr Loretta Universal Glow Daily Defense SPF 40

NDC 71501-1910, ZINC OXIDE, cream, from Dr. Loretta, LLC.

Product NDC
71501-1910
Status
Listed
Labeler
Dr. Loretta, LLC
Dosage form
CREAM
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M020
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71501-1910 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ZINC OXIDE170 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
71501-1910-1715011910011.5 mL in 1 PACKET (71501-1910-1)
71501-1910-271501191002100 mL in 1 BOTTLE, PUMP (71501-1910-2)
71501-1910-3715011910031 BOTTLE, PUMP in 1 BOX (71501-1910-3) / 10 mL in 1 BOTTLE, PUMP

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 71501-1910 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71501-1910 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71501-1910. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.