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DR.JART EVERY SUN DAY SUN FLUID

NDC 49404-154, homosalate, octinoxate, octisalate, octocrylene, avobenzone, liquid, from Have & Be Co., Ltd..

Product NDC
49404-154
Status
Listed
Labeler
Have & Be Co., Ltd.
Dosage form
LIQUID
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/49404-154 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OCTINOXATE68 mg/mL
  • OCTOCRYLENE40 mg/mL
  • HOMOSALATE90 mg/mL
  • AVOBENZONE29 mg/mL
  • OCTISALATE45 mg/mL
Package NDCNDC-11Package
49404-154-01494040154011 CONTAINER in 1 CARTON (49404-154-01) / 100 mL in 1 CONTAINER

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 49404-154 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49404-154 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49404-154. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.