Biossance Squalane Moisturizer
- Product NDC
- 73517-381
- Requested package NDC
- 73517-381-01
- 11-digit product format
- 735170381
- Labeler code
- 73517
- Product ID
- 73517-381_ec976a81-09f3-6fb6-e053-2995a90a46e2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Amyris, Inc
- Application
- M020
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-06-01
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 14 g/100mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 73517-381 | 73517-381-01 | D | Discontinued by firm | 2026-10-21 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Code | Status | Snapshot | Source SHA-256 |
|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | D | Discontinued by firm | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 73517-381-01 | 2025-12-01 | ee62c442-742f-44e9-b58b-e3d901bc9555 |
| 73517-381-02 | 2025-12-01 | ee62c442-742f-44e9-b58b-e3d901bc9555 |
| 73517-381-03 | 2025-12-01 | ee62c442-742f-44e9-b58b-e3d901bc9555 |
| 73517-381-01 | 2025-01-30 | ee62c442-742f-44e9-b58b-e3d901bc9555 |
| 73517-381-02 | 2025-01-30 | ee62c442-742f-44e9-b58b-e3d901bc9555 |
| 73517-381-03 | 2025-01-30 | ee62c442-742f-44e9-b58b-e3d901bc9555 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 73517-381-01 | 73517038101 | 1 TUBE in 1 CARTON (73517-381-01) > 20 mL in 1 TUBE | 1 tube | 2020-06-01 | 0000-00-00 | No | No | Current |