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SunDrops 75

NDC 63621-356, Alcohol, gel, from Sunburst Chemicals, Inc..

Product NDC
63621-356
Status
Listed
Labeler
Sunburst Chemicals, Inc.
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
505G(a)(3)
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63621-356 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALCOHOL.6 mL/mL
Package NDCNDC-11Package
63621-356-14636210356143785 mL in 1 BOTTLE, PLASTIC (63621-356-14)
63621-356-20636210356208 BAG in 1 BOX (63621-356-20) / 1000 mL in 1 BAG
63621-356-256362103562512 BOTTLE, PUMP in 1 BOX (63621-356-25) / 236.6 mL in 1 BOTTLE, PUMP
63621-356-40636210356404 BAG in 1 BOX (63621-356-40) / 1000 mL in 1 BAG
63621-356-5063621035650473.2 mL in 1 BOTTLE, PUMP (63621-356-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

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

Use it

Look up 63621-356 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63621-356 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63621-356. 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.